Compositions

ABSTRACT

There is provided inter alia a composition comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide.

This application is a continuation-in-part of International Application No. PCT/EP2017/074828 filed Sep. 29, 2017, which claims priority to European Application No. 16191988.1 filed Sep. 30, 2016, the contents of which are incorporated herewith in their entirety.

FIELD OF THE INVENTION

The present invention relates to compositions and constructs comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide. The present invention also relates to nucleic acids encoding such constructs, to methods for preparing such compositions and constructs, to cDNA and vectors comprising nucleic acids encoding such constructs, to host cells expressing or capable of expressing such constructs and to uses of such compositions and constructs.

BACKGROUND OF THE INVENTION

Tumour necrosis factor-alpha is a homotrimeric pro-inflammatory cytokine involved in systemic inflammation which exists in both soluble and membrane-bound forms. TNF-alpha is secreted predominantly by monocytes and macrophages but is also secreted by tumour cell lines as well as CD4+ and CD8+ peripheral blood T lymphocytes and some cultured T and B cell lines. TNF-alpha has been implicated in inflammatory diseases, autoimmune diseases, viral, bacterial and parasitic infections, malignancies, and/or neurodegenerative diseases and is a target for specific biological therapy in autoimmune/autoinflammatory diseases such as rheumatoid arthritis and Crohn's disease. A TNF-alpha inhibitor which has sufficient specificity to TNF-alpha may be an efficient prophylactic or therapeutic pharmaceutical for preventing or treating diseases such as Crohn's disease, where TNF-alpha has been implicated as a key cytokine driving the pathology observed.

IL-6 induces cell activation via a receptor system that consists of two receptor chains: a ligand-specific non-signalling transmembrane IL-6 receptor alpha subunit (the membrane-bound form of IL-6R, also known as mIL-6R, IL-6Ra, gp80 and CD126) and a second trans-membrane receptor chain gp130 that is required for signal transduction. In classical (cis) IL-6 signalling, IL-6 first binds to the membrane IL-6Ra subunit, which in turn associates with gp130 to form an IL-6-receptor complex that is able to induce cell activation. The restricted expression of membrane IL-6Ra receptors limits this classical IL-6 signalling mechanism to a few cell types including hepatocytes, neutrophils, monocyte/macrophages, some lymphocyte subtypes and intestinal epithelial cells. A second form of the IL-6R comprising the extracellular ligand-binding region of the IL-6Ra-subunit has also been identified. The soluble form of the IL-6R (sIL-6R) is generated by protease mediated shedding of IL-6Rα ecto-domains from membrane IL-6R expressing cells or is secreted from the cells as an alternatively spliced product. Importantly, IL-6 can still bind to the sIL-6R and the IL-6/sIL-6R complexes formed can associate with gp130-receptor chains to induce signalling. As a wide range of cells express gp130 but not the IL-6R, this process termed “trans-signalling” provides a mechanism for extending the range of cell types that are capable of responding to IL-6 and this process appears to be particularly important for the development and perpetuation of chronic inflammation (Rose-John 2012). Inhibition of the IL-6R has potential for therapeutic benefit in autoimmune diseases such as Crohn's disease (CD) and ulcerative colitis (UC). Systemically administered IL-6 pathway antagonists including both IL-6 and IL-6R blocking antibodies have demonstrated efficacy without major toxicity in inflammatory diseases including rheumatoid arthritis and Castleman's disease. Tocilizumab, a humanised IL-6R monoclonal antibody that targets both membrane and soluble IL-6Rs (cis/trans signalling inhibitor) has also shown evidence of clinical efficacy in a pilot clinical study in patients with Crohn's disease (Ito et al., 2004).

TNF-alpha and IL-6 are both therefore cytokines that regulate cell types and pathways involved in the development and maintenance of intestinal inflammation in IBD. Although the relative contributions of these cytokines to different disease processes are unclear, the results of clinical studies have shown that antibodies that antagonise the actions of either TNF-alpha or IL-6/IL-6R signalling are effective in Crohn's patients. However, these antibodies have limited efficacy. Accordingly, there exists today a need for improved IBD therapeutics.

WO2004041862, WO2006122786 and Coppieters et al 2006 (herein incorporated by reference in their entirety) disclose single domain antibodies directed against TNF-alpha and related aspects. The sequence referred to in WO 2006/122786 as “TNF1”, “PMP1C2” or “SEQ ID NO: 52”) is characterised further below.

WO2008020079, WO2008071685, WO2009095489, WO2010115995, WO2010115998 and WO2013041722 (herein incorporated by reference in their entirety) disclose single domain antibodies directed against IL-6R and related aspects. The sequence referred to in WO2010115998 as “20A11” or “SEQ ID NO: 66” is characterised further below.

WO2015065987 (herein incorporated by reference in its entirety) discloses a bispecific antibody comprising at least one anti-TNF-alpha antibody or antigen-binding fragment thereof and at least one anti-IL-6 antibody or antigen-binding fragment thereof.

Compositions or constructs of the present invention may, in at least some embodiments, have one or more of the following advantages compared to substances of the prior art. These advantages may be realised by each of the component polypeptides in a composition of the invention in their own right, or alternatively the combination of the polypeptides in a composition of the invention may result in an additive or even synergistic effect in respect of one or more of the below advantages.

-   -   (a) increased affinity and/or avidity for TNF-alpha and/or         IL-6R;     -   (b) increased specificity for TNF-alpha and/or IL-6R;     -   (c) increased neutralising capability against TNF-alpha and/or         IL-6R;     -   (d) increased inhibition of phosphorylation of signalling         proteins;     -   (e) increased inhibition of cytokine production;     -   (f) increased cross-reactivity with TNF-alpha and/or IL-6R from         different species such as human and cynomolgus monkey;     -   (g) increased cross-reactivity with both soluble and membrane         forms of TNF-alpha;     -   (h) reduced immunogenicity, for example when administered to a         mouse, cynomolgus monkey or human;     -   (i) increased stability in the presence of proteases, for         example (a) in the presence of proteases found in the small         and/or large intestine and/or IBD inflammatory proteases, for         example trypsin, chymotrypsin, enterokinase, MMP3, MMP10, MMP12,         other MMPs and cathepsin and/or (b) in the presence of proteases         such as cell membrane-attached proteases, secreted proteases and         proteases released on cell lysis from gut commensal microflora         and/or pathogenic bacteria, found in the small and/or large         intestine;     -   (j) increased stability to protease degradation during         production (for example resistance to yeast proteases);     -   (k) increased suitability for oral administration;     -   (l) increased suitability for local delivery to the intestinal         tract and lamina propria following oral administration;     -   (m) increased suitability for expression in a heterologous host         such as bacteria (e.g. Escherichia coli) or a yeast (e.g.         Saccharomyces cerevisiae);     -   (n) suitability for, and improved properties for, use in a         pharmaceutical;     -   (o) suitability for, and improved properties for, use in a         functional food;     -   (p) improved tissue penetration such as penetration of inflamed         colonic mucosal epithelium and submucosal tissues to access the         sub mucosal lamina propria;     -   (q) decreased immunogenicity in humans for example due to         increased sequence similarity to human immunoglobulins;     -   (r) more effective prevention or treatment of autoimmune disease         and/or inflammatory disease, including amelioration of the         symptoms thereof, including in particular inflammatory bowel         disease and/or mucositis, particularly when administered orally;     -   (s) binding to novel epitopes.

SUMMARY OF THE INVENTION

The present inventors have provided surprisingly effective compositions comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide. In particular, it has been found that the provision of a TNF-alpha binding polypeptide and an IL-6R binding polypeptide in a single composition may be more effective than the provision of each binding polypeptide separately. In some embodiments, the combination of these polypeptides in compositions of the invention may have an additive effect and in further embodiments, the combination of these polypeptides in compositions of the invention may have a synergistic effect.

Based on the findings disclosed herein using ex vivo cultured intestinal mucosal tissue from inflammatory bowel disease patients (Examples 10 and 11) it may be expected that these compositions have particular utility in the prevention or treatment of autoimmune and or inflammatory disease. More specifically, the findings disclosed herein indicate that these compositions may have particular utility in the prevention or treatment of inflammatory bowel disease (for example Crohn's disease or ulcerative colitis), or in the prevention or treatment of mucositis, particularly when administered orally.

It may be expected that the same benefits may be derived by the use of a TNF-alpha binding polypeptide in the treatment or prevention of disease, together with an IL-6R binding polypeptide, wherein the polypeptides are not combined in the same composition. Similarly, it may be expected that the same benefits may be derived by the use of an IL-6R binding polypeptide in the treatment or prevention of disease, together with a TNF-alpha binding polypeptide, wherein the polypeptides are not combined in the same composition.

The present invention provides a composition comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide.

Also provided is a construct comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide, and a polynucleotide encoding said construct.

Also provided is a TNF-alpha binding polypeptide for use in the treatment or prevention of an autoimmune disease and/or inflammatory disease, together with an IL-6R binding polypeptide; and an IL-6R binding polypeptide for use in the treatment or prevention of an autoimmune disease and/or inflammatory disease, together with a TNF-alpha binding polypeptide.

Many of the specific TNF-alpha binding polypeptides, the specific IL-6R binding polypeptides and the data disclosed herein are also disclosed in particular earlier-filed patent applications. These include PCT application number PCT/EP2016/057021 (which is incorporated herein by reference in its entirety, particularly in so far as the application relates to the TNF-alpha binding polypeptide ID-38F) and EP application number 16152321.2 and PCT application number PCT/EP2017/051237 (which are incorporated herein by reference in their entirety, particularly in so far as the applications relate to the IL-6R binding polypeptide ID-142V).

DESCRIPTION OF THE FIGURES

FIG. 1—Potency of ID-38F compared to TNF-alpha binding polypeptides of the prior art (L929 assay)

FIG. 2—Effects of TNF-alpha and IL-6R neutralising ICVDs, alone and in combination, on phosphoproteins in Crohn's biopsy tissue (phosphoprotein signal)

FIG. 3—Inhibition of phosphoproteins in Crohn's biopsy tissue by TNF-alpha and IL-6R neutralising ICVDs, alone and in combination (inhibition vs control (%))

FIG. 4—Effects of TNF-alpha and IL-6R neutralising ICVDs, alone and in combination, on phosphoproteins in ulcerative colitis biopsy tissue (phosphoprotein signal)

FIG. 5—Effects of TNF-alpha and IL-6R neutralising ICVDs, alone and in combination, on Crohn's biopsy tissue cytokine production (cytokine concentration (pg/ml))

FIG. 6—Effects of TNF-alpha and IL-6R neutralising ICVDs, alone and in combination, on Crohn's biopsy tissue cytokine production, relative to control (cytokine production (% control))

FIG. 7—Polyacrylamide gel image demonstrating liberation of ID-38F and ID-142V from heterobihead constructs comprising a labile linker

FIG. 8—Polyacrylamide gel image demonstrating stability of non-labile linker used in heterobihead construct ID-11K

DESCRIPTION OF THE SEQUENCES

SEQ ID NO: 1—Polypeptide sequence of CDR1 of ID-38F

SEQ ID NO: 2—Polypeptide sequence of CDR2 of ID-38F

SEQ ID NO: 3—Polypeptide sequence of CDR3 of ID-38F

SEQ ID NO: 4—Polypeptide sequence of FR1 of ID-38F

SEQ ID NO: 5—Polypeptide sequence of FR2 of ID-38F

SEQ ID NO: 6—Polypeptide sequence of FR3 of ID-38F

SEQ ID NO: 7—Polypeptide sequence of FR4 of ID-38F

SEQ ID NO: 8—Polypeptide sequence of ID-38F

SEQ ID NO: 9—Polypeptide sequence of CDR1 of ID-142V

SEQ ID NO: 10—Polypeptide sequence of CDR2 of ID-142V

SEQ ID NO: 11—Polypeptide sequence of CDR3 of ID-142V

SEQ ID NO: 12—Polypeptide sequence of FR1 of ID-142V

SEQ ID NO: 13—Polypeptide sequence of FR2 of ID-142V

SEQ ID NO: 14—Polypeptide sequence of FR3 of ID-142V

SEQ ID NO: 15—Polypeptide sequence of FR4 of ID-142V

SEQ ID NO: 16—Polypeptide sequence of ID-142V

SEQ ID NO: 17—Polynucleotide sequence encoding ID-38F

SEQ ID NO: 18—Polynucleotide sequence encoding ID-142V

SEQ ID NO: 19—Polypeptide sequence of ID-9K including export signal sequence

SEQ ID NO: 20—Polypeptide sequence of ID-10K including export signal sequence

SEQ ID NO: 21—Polypeptide sequence of ID-11K including export signal sequence

SEQ ID NO: 22—Polypeptide sequence of ID-12K including export signal sequence

SEQ ID NO: 23—Polypeptide sequence of ID-13K including export signal sequence

SEQ ID NO: 24—Polypeptide sequence of ID-14K including export signal sequence

SEQ ID NO: 25—Polynucleotide sequence encoding SEQ ID NO: 19

SEQ ID NO: 26—Polynucleotide sequence encoding SEQ ID NO: 20

SEQ ID NO: 27—Polynucleotide sequence encoding SEQ ID NO: 21

SEQ ID NO: 28—Polynucleotide sequence encoding SEQ ID NO: 22

SEQ ID NO: 29—Polynucleotide sequence encoding SEQ ID NO: 23

SEQ ID NO: 30—Polynucleotide sequence encoding SEQ ID NO: 24

SEQ ID NO: 31—Polypeptide sequence of enterokinase cleavage site

SEQ ID NO: 32—Polypeptide sequence of specific labile linker used in ID-9K and ID-10K

SEQ ID NO:33—Polypeptide sequence of specific non-labile linker used in ID-11K

SEQ ID NO: 34—Polypeptide sequence of ID-123V

DETAILED DESCRIPTION OF THE INVENTION

Polypeptides Such as Antibodies and Antibody Fragments Including Immunoglobulin Chain Variable Domains (ICVDs) Such as the VH and VHH

Polypeptides are organic polymers consisting of a number of amino acid residues bonded together in a chain. As used herein, ‘polypeptide’ is used interchangeably with ‘protein’ and ‘peptide’. Polypeptides are said to be binding polypeptides when they contain one or more stretches of amino acid residues which form a binding site, capable of binding to an epitope on a target, with an affinity (suitably expressed as a Kd value, a Ka value, a k_(on)-rate and/or a k_(off)-rate, as further described herein).

Binding polypeptides include polypeptides such as DARPins (Binz et al. 2003), Affimers™ (Johnson et al 2012), Fynomers™ (Grabulovski et al 2007), Centyrins (Goldberg et al 2016), Affitins (e.g. Nanofitins®, Krehenbrink et al 2008), cyclic peptides, antibodies and antibody fragments. Binding polypeptides also include polypeptides such as Affibodies (Nygren 2008), Affilins (Ebersbach et al. 2007), Alphabodies (Desmet et al 2014), Anticalins (Skerra et al 2008), Avimers (Silverman et al 2005), Kunitz domain peptides (Nixon and Wood 2006), Monobodies (Koide and Koide 2007), nanoCLAMPs (Suderman et al 2017), Adnectins (Lipovsek 2011) and bicyclic peptides.

A conventional antibody or immunoglobulin (Ig) is a protein comprising four polypeptide chains: two heavy (H) chains and two light (L) chains. Each chain is divided into a constant region and a variable domain. The heavy chain variable domains are abbreviated herein as VHC, and the light (L) chain variable domains are abbreviated herein as VLC. These domains, domains related thereto and domains derived therefrom, are referred to herein as immunoglobulin chain variable domains.

The VHC and VLC domains can be further subdivided into regions of hypervariability, termed “complementarity determining regions” (“CDRs”), interspersed with regions that are more conserved, termed “framework regions” (“FRs”). The framework and complementarity determining regions have been precisely defined (Kabat et al 1991 Sequences of Proteins of Immunological Interest, Fifth Edition U.S. Department of Health and Human Services, NIH Publication Number 91-3242, herein incorporated by reference in its entirety). In a conventional antibody, each VHC and VLC is composed of three CDRs and four FRs, arranged from amino-terminus to carboxy-terminus in the following order: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4. The conventional antibody tetramer of two heavy immunoglobulin chains and two light immunoglobulin chains is formed with the heavy and the light immunoglobulin chains inter-connected by e.g. disulfide bonds, and the heavy chains similarity connected. The heavy chain constant region includes three domains, CH1, CH2 and CH3. The light chain constant region is comprised of one domain, CL.

The variable domain of the heavy chains and the variable domain of the light chains are binding domains that interact with an antigen. The constant regions of the antibodies typically mediate the binding of the antibody to host tissues or factors, including various cells of the immune system (e.g. effector cells) and the first component (C1q) of the classical complement system. The term antibody includes immunoglobulins of types IgA, IgG, IgE, IgD, IgM (as well as subtypes thereof), wherein the light chains of the immunoglobulin may be kappa or lambda types. The overall structure of immunoglobulin-gamma (IgG) antibodies assembled from two identical heavy (H)-chain and two identical light (L)-chain polypeptides is well established and highly conserved in mammals (Padlan 1994 Mol Immunol 31:169-217).

An exception to conventional antibody structure is found in sera of Camelidae. In addition to conventional antibodies, these sera possess special IgG antibodies. These IgG antibodies, known as heavy-chain antibodies (HCAbs), are devoid of the L chain polypeptide and lack the first constant domain (CH1). At its N-terminal region, the H chain of the homodimeric protein contains a dedicated immunoglobulin chain variable domain, referred to as the VHH, which serves to associate with its cognate antigen (Muyldermans et al 2013, Hamers-Casterman et al 1993, Muyldermans et al 1994, herein incorporated by reference in their entirety).

An antibody fragment as used herein refers to a portion of an antibody that specifically binds to a target (e.g. a molecule in which one or more immunoglobulin chains is not full length, but which specifically binds to a target). Examples of binding fragments encompassed within the term antibody fragment (or ‘antigen-binding fragment’) include:

(i) a Fab fragment (a monovalent fragment consisting of the VLC, VHC, CL and CH1 domains);

(ii) a F(ab′)2 fragment (a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region);

(iii) a Fd fragment (consisting of the VHC and CH1 domains);

(iv) a Fv fragment (consisting of the VLC and VHC domains of a single arm of an antibody);

(v) an scFv fragment (consisting of VLC and VHC domains joined, using recombinant methods, by a synthetic linker that enables them to be made as a single protein chain in which the VLC and VHC regions pair to form monovalent molecules);

(vi) a VH (an immunoglobulin chain variable domain consisting of a VHC domain (Ward et al 1989);

(vii) a VL (an immunoglobulin chain variable domain consisting of a VLC domain);

(viii) a V-NAR (an immunoglobulin chain variable domain consisting of a VHC domain from chondrichthyes IgNAR (Roux et al 1998 and Griffiths et al 2013, herein incorporated by reference in their entirety)

(ix) a VHH.

The total number of amino acid residues in a VHH or VH may be in the region of 110-140, more suitably 112-120.

The examples provided herein relate to compositions comprising immunoglobulin chain variable domains which bind to TNF-alpha and immunoglobulin chain variable domains which bind to IL-6R. The principles of the invention disclosed herein are, however, equally applicable to any compositions comprising polypeptides which bind to TNF-alpha and polypeptides which bind to IL-6R, such as antibodies and antibody fragments. For example, immunoglobulin chain variable domains may be incorporated into a polypeptide such as a full length antibody. Such an approach is demonstrated by McCoy et al., 2014, who provide an anti-HIV VHH engineered as a fusion with a human Fc region (including hinge, CH2 and CH3 domains), expressed as a dimer construct.

Specificity, Affinity, Avidity, Potency, Inhibition and Neutralisation

Specificity refers to the number of different targets (such as antigens or antigenic determinants) to which a particular binding polypeptide can bind. The specificity of a binding polypeptide is the ability of the binding polypeptide to recognise a particular target as a unique molecular entity and distinguish it from another.

Affinity, represented by the equilibrium constant for the dissociation of a target from a binding polypeptide (Kd), is a measure of the binding strength between a target and a binding site on a binding polypeptide: the lesser the value of the Kd, the stronger the binding strength between a target and the binding polypeptide (alternatively, the affinity can also be expressed as the affinity constant (Ka), which is 1/Kd). Affinity can be determined by known methods, depending on the specific antigen of interest. Suitably, affinity is determined using a dynamically switchable biosurface (e.g. “switchSENSE®”, see Knezevic et al 2012) or by surface plasmon resonance.

Avidity is the measure of the strength of binding between a binding polypeptide and the pertinent target. Avidity is related to both the affinity between a target and its binding site on the binding polypeptide and the number of pertinent binding sites present on the binding polypeptide.

Any Kd value less than 10⁻⁶ is considered to indicate binding. Specific binding of a binding polypeptide to a target (such as an antigen or antigenic determinant) can be determined in any suitable known manner, including, for example, Scatchard analysis and/or competitive binding assays, such as radioimmunoassays (RIA), enzyme immunoassays (EIA) and sandwich competition assays, and the different variants thereof known in the art.

Potency is a measure of the activity of a therapeutic agent (such as a binding polypeptide) expressed in terms of the amount required to produce an effect of given intensity. A highly potent agent evokes a greater response at low concentrations compared to an agent of lower potency that evokes a smaller response at low concentrations. Potency is a function of affinity and efficacy. Efficacy refers to the ability of therapeutic agent to produce a biological response upon binding to a target and the quantitative magnitude of this response. The term half maximal effective concentration (EC50) refers to the concentration of a therapeutic agent which causes a response halfway between the baseline and maximum after a specified exposure time. The therapeutic agent may cause inhibition (which may be referred to specifically as half maximal inhibitory concentration, ‘IC50’) or stimulation. EC50 and IC50 are commonly used, and are used herein, as a measure of potency. EC50 and IC50 are used interchangeably herein in respect of the TNF-alpha binding polypeptides and IL-6R binding polypeptides, due to both binding polypeptides causing inhibition of a target.

Specific assays which are suitable for ascertaining the potency of TNF-alpha binding polypeptides and IL-6R binding polypeptides are detailed below under the headings ‘TNF-alpha binding polypeptides’ and ‘IL-6R binding polypeptides’, respectively.

Polypeptide and Polynucleotide Sequences

For the purposes of comparing two closely-related polypeptide sequences, the “% sequence identity” between a first polypeptide sequence and a second polypeptide sequence may be calculated using NCBI BLAST v2.0, using standard settings for polypeptide sequences (BLASTP). For the purposes of comparing two closely-related polynucleotide sequences, the “% sequence identity” between a first nucleotide sequence and a second nucleotide sequence may be calculated using NCBI BLAST v2.0, using standard settings for nucleotide sequences (BLASTN).

Polypeptide or polynucleotide sequences are said to be the same as or identical to other polypeptide or polynucleotide sequences, if they share 100% sequence identity over their entire length. Residues in sequences are numbered from left to right, i.e. from N- to C-terminus for polypeptides; from 5′ to 3′ terminus for polynucleotides.

A “difference” between sequences refers to an insertion, deletion or substitution of a single amino acid residue in a position of the second sequence, compared to the first sequence. Two polypeptide sequences can contain one, two or more such amino acid differences. Insertions, deletions or substitutions in a second sequence which is otherwise identical (100% sequence identity) to a first sequence result in reduced % sequence identity. For example, if the identical sequences are 9 amino acid residues long, one substitution in the second sequence results in a sequence identity of 88.9%. If the identical sequences are 17 amino acid residues long, two substitutions in the second sequence results in a sequence identity of 88.2%. If the identical sequences are 7 amino acid residues long, three substitutions in the second sequence results in a sequence identity of 57.1%. If first and second polypeptide sequences are 9 amino acid residues long and share 6 identical residues, the first and second polypeptide sequences share greater than 66% identity (the first and second polypeptide sequences share 66.7% identity). If first and second polypeptide sequences are 17 amino acid residues long and share 16 identical residues, the first and second polypeptide sequences share greater than 94% identity (the first and second polypeptide sequences share 94.1% identity). If first and second polypeptide sequences are 7 amino acid residues long and share 3 identical residues, the first and second polypeptide sequences share greater than 42% identity (the first and second polypeptide sequences share 42.9% identity).

Alternatively, for the purposes of comparing a first, reference polypeptide sequence to a second, comparison polypeptide sequence, the number of additions, substitutions and/or deletions made to the first sequence to produce the second sequence may be ascertained. An addition is the addition of one amino acid residue into the sequence of the first polypeptide (including addition at either terminus of the first polypeptide). A substitution is the substitution of one amino acid residue in the sequence of the first polypeptide with one different amino acid residue. A deletion is the deletion of one amino acid residue from the sequence of the first polypeptide (including deletion at either terminus of the first polypeptide).

A “conservative” amino acid substitution is an amino acid substitution in which an amino acid residue is replaced with another amino acid residue of similar chemical structure and which is expected to have little influence on the function, activity or other biological properties of the polypeptide. Such conservative substitutions suitably are substitutions in which one amino acid within the following groups is substituted by another amino acid residue from within the same group:

Group Amino acid residue Non-polar Glycine aliphatic Alanine Valine Leucine Isoleucine Aromatic Phenylalanine Tyrosine Tryptophan Polar Serine uncharged Threonine Asparagine Glutamine Negatively Aspartate charged Glutamate Positively Lysine charged Arginine

Suitably, a hydrophobic amino acid residue is a non-polar amino acid. More suitably, a hydrophobic amino acid residue is selected from V, I, L, M, F, W or C.

As used herein, numbering of polypeptide sequences and definitions of CDRs and FRs are as defined according to the Kabat system (Kabat et al 1991 Sequences of Proteins of Immunological Interest, Fifth Edition U.S. Department of Health and Human Services, NIH Publication Number 91-3242, herein incorporated by reference in its entirety). A “corresponding” amino acid residue between a first and second polypeptide sequence is an amino acid residue in a first sequence which shares the same position according to the Kabat system with an amino acid residue in a second sequence, whilst the amino acid residue in the second sequence may differ in identity from the first. Suitably corresponding residues will share the same number (and letter) if the framework and CDRs are the same length according to Kabat definition. Alignment can be achieved manually or by using, for example, a known computer algorithm for sequence alignment such as NCBI BLAST v2.0 (BLASTP or BLASTN) using standard settings.

The Kabat numbering system is applied below to particular TNF-alpha and IL-6R binding polypeptides used in the examples provided herein.

The Kabat Numbering System Applied to ID-142V, an IL-6R Binding Polypeptide

The CDRs of the ID-142V polypeptide labelled below as ‘CDR-H1’, ‘CDR2-H2’ and ‘CDR-H3’ relate to ‘CDR1’, ‘CDR2’ and ‘CDR3’ respectively, as discussed herein. Numbering in the ID-142V figure below with the prefix ‘H’ is Kabat numbering, while numbering below the amino acid sequence is numbering of amino acids consecutively from N- to C-terminus. The residues of each CDR or FR can also be numbered from the N- to the C-terminus of that CDR or FR.

H1 H2 H3 H4 H5 H6 H7 H8 H9 H10 H11 H12 H13 ID-142V D V Q L V E S G G G L V Q 1 2 3 4 5 6 7 8 9 10 11 12 13 H14 H15 H16 H17 H18 H19 H20 H21 H22 H23 H24 H25 H26 A G G S T R L T C K A S G 14 15 16 17 18 19 20 21 22 23 24 25 26 CDR-H1 H27 H28 H29 H29A H29B H29C H30 H31 H32 H33 H34 H35 H36 S I S N I N S I N V M A W 27 28 29 30 31 32 33 34 35 36 37 38 39 H37 H38 H39 H40 H41 H42 H43 H44 H45 H46 H47 H48 H49 Y R Q A P G K G R E L V A 40 41 42 43 44 45 46 47 48 49 50 51 52 CDR2-H2 H50 H51 H52 H53 H54 H55 H56 H57 H58 H59 H60 H61 H62 I I G K G G G T N Y A D F 53 54 55 56 57 58 59 60 61 62 63 64 65 H63 H4 H65 H66 H67 H68 H69 H70 H71 H72 H73 H74 H75 V K G R F T I S R D A A K 66 67 68 69 70 71 72 73 74 75 76 77 78 H76 H77 H78 H79 H80 H81 H82 H82A H82B H82C H83 H84 H85 N T V Y L Q M N S L R P E 79 80 81 82 83 84 85 86 87 88 89 90 91 CDR-H3 H86 H87 H88 H89 H90 H91 H92 H93 H94 H95 H96 H97 H98 D T A V Y Y C Y A D Y E D 92 93 94 95 96 97 98 99 100 101 102 103 104 CDR-H3 H99 H100 H100A H100B H100C H100D H101 H102 H103 H104 H105 H106 H107 H D S P H N A S W G Q G T 105 106 107 108 109 110 111 112 113 114 115 116 117 H108 H109 H110 H111 H112 H113 Q V T V S S 118 119 120 121 122 123

Region FR1 FR1 FR1 FR1 FR1 FR1 FR1 FR1 FR1 FR1 FR1 Residue # 1 2 3 4 5 6 7 8 9 10 11 ID38F D V Q L V E S G G G L Kabat H1 H2 H3 H4 H5 H6 H7 H8 H9 H10 H11 numbering Region FR1 FR1 FR1 FR1 FR1 FR1 FR1 FR1 FR1 FR1 Residue # 12 13 14 15 16 17 18 19 20 21 ID38F V Q P G G S L K L S Kabat H12 H13 H14 H15 H16 H17 H18 H19 H20 H21 numbering Region FR1 FR1 FR1 FR1 FR1 FR1 FR1 FR1 FR1 CDR1 CDR1 Residue # 22 23 24 25 26 27 28 29 30 31 32 ID38F C A A S G F D F S S H Kabat H22 H23 H24 H25 H26 H27 H28 H29 H30 H31 H32 numbering Region CDR1 CDR1 CDR1 FR2 FR2 FR2 FR2 FR2 FR2 FR2 Residue # 33 34 35 36 37 38 39 40 41 42 ID38F W M Y W V R Q A P G Kabat H33 H34 H35 H36 H37 H38 H39 H40 H41 H42 numbering Region FR2 FR2 FR2 FR2 FR2 FR2 FR2 CDR2 CDR2 CDR2 CDR2 Residue # 43 44 45 46 47 48 49 50 51 52 53 ID38F K E L E W L S E I N T Kabat H43 H44 H45 H46 H47 H48 H49 H50 H51 H52 H52A numbering Region CDR2 CDR2 CDR2 CDR2 CDR2 CDR2 CDR2 CDR2 CDR2 CDR2 Residue # 54 55 56 57 58 59 60 61 62 63 ID38F N G L I T H Y G D S Kabat H53 H54 H55 H56 H57 H58 H59 H60 H61 H62 numbering Region CDR2 CDR2 CDR2 FR3 FR3 FR3 FR3 FR3 FR3 FR3 FR3 Residue # 64 65 66 67 68 69 70 71 72 73 74 ID38F V K G R F T V S R N N Kabat H63 H64 H65 H66 H67 H68 H69 H70 H71 H72 H73 numbering Region FR3 FR3 FR3 FR3 FR3 FR3 FR3 FR3 FR3 FR3 Residue # 75 76 77 78 79 80 81 82 83 84 ID38F A A N K M Y L E L T Kabat H74 H75 H76 H77 H78 H79 H80 H81 H82 H82A numbering Region FR3 FR3 FR3 FR3 FR3 FR3 FR3 FR3 FR3 FR3 FR3 Residue # 85 86 87 88 89 90 91 92 93 94 95 ID38F R L E P E D T A L Y Y Kabat H82B H82C H83 H84 H85 H86 H87 H88 H89 H90 H91 numbering Region FR3 FR3 FR3 CDR3 CDR3 CDR3 CDR3 CDR3 CDR3 FR4 Residue # 96 97 98 99 100 101 102 103 104 105 ID38F C A R N Q H G L N K Kabat H92 H93 H94 H95 H96 H97 H98 H101 H102 H103 numbering Region FR4 FR4 FR4 FR4 FR4 FR4 FR4 FR4 FR4 FR4 Residue # 106 107 108 109 110 111 112 113 114 115 ID38F G Q G T Q V T V S S Kabat H104 H105 H106 H107 H108 H109 H110 H111 H112 H113 numbering

Numbering in the ID-38F figure above with the prefix ‘H’ is Kabat numbering, while numbering above the amino acid sequence is numbering of amino acids consecutively from to C-terminus. The residues of each CDR or FR can also be numbered from the N- to the C-terminus of that CDR or FR.

Features of the polynucleotide sequences disclosed herein are as follows:

DNA base Start End of Start encoded encoded Sequence identifier signal binding binding number and encoded sequence polypeptide polypeptide Stop polypeptide (ATG) (GAT) (A of TCA) codon 25, ID9K and export 33 288 1034 1035-7 signal sequence 26, ID10K and export 33 288 1034 1035-7 signal sequence 27, ID11K and export 33 288 1091 1092-4 signal sequence 28, ID12K and export 33 288 1091 1092-4 signal sequence 29, ID13K and export 33 288 1031 1032-4 signal sequence 30, ID14K and export 33 288 1061 1062-4 signal sequence 17, ID-38F 82 337 681  682-4 18, ID-142V 42 297 665  666-8

Suitably, the polynucleotides used in the present invention are isolated. An “isolated” polynucleotide is one that is removed from its original environment. For example, a naturally-occurring polynucleotide is isolated if it is separated from some or all of the coexisting materials in the natural system. A polynucleotide is considered to be isolated if, for example, it is cloned into a vector that is not a part of its natural environment or if it is comprised within cDNA.

TNF-Alpha Binding Polypeptides

Functional Properties

An anti-TNF-alpha polypeptide, a polypeptide which interacts with TNF-alpha, or a polypeptide against TNF-alpha, are all effectively TNF-alpha binding polypeptides. A TNF-alpha binding polypeptide may bind to a linear or conformational epitope on TNF-alpha. Suitably the TNF-alpha binding polypeptide binds to human TNF-alpha.

Suitably, the TNF-alpha binding polypeptide binds to TNF-alpha with an equilibrium dissociation constant (Kd) of 10⁻⁶ M or less, more suitably 10⁻⁷ M or less, more suitably 10⁻⁸ M or less and more suitably 10⁻⁹ M or less.

Suitably the affinity of the TNF-alpha binding polypeptide is determined using a dynamically switchable biosurface (e.g. “switchSENSE®”, see Knezevic et al 2012).

In one embodiment, the affinity of the TNF-alpha binding polypeptide is established at 25° C. by fusing the TNF-alpha binding polypeptide at its C-terminus to single stranded DNA and coupling the DNA-polypeptide fusion to a gold-electrode coated in the fluorescently-labelled complementary strand of single-stranded DNA, before exposing the chip-bound TNF-alpha binding polypeptide to a 10 kHz electrical current and human TNF-alpha at five different concentrations between 50 pM and 4.5 nM for 600 seconds and observing dissociation for 8 hours by time resolved fluorescence.

Suitably the TNF-alpha binding polypeptide neutralises TNF-alpha. A TNF-alpha-neutralising polypeptide is a polypeptide which defends a cell from the effects of TNF-alpha by, for example, inhibiting the biological effect of TNF-alpha. Conventionally, anti-TNF-alpha therapeutic antibody products have used an L929 murine cell line with a cell death endpoint as a neutralisation assay (Humphreys and Wilson 1999). An L929 assay can be performed (as demonstrated in Example 1) to assay the ability of a TNF-alpha binding polypeptide to neutralise the effects of TNF-alpha cytotoxicity by ascertaining the half maximal effective concentration (EC50) of the TNF-alpha binding polypeptide. A detailed protocol for the L929 assay is provided below.

L929 Assay

L929 cells (10000 cells/well) are cultured for 24 h in the presence of soluble TNF-alpha (500 pg/ml) and actinomycin (0.75 ug/mL) together with dilutions of the purified polypeptides. At the end of the experiment cytotoxicity is determined using resazurin. The inhibition of soluble human TNF-induced cytotoxicity of mouse L929 cells is tested to determine TNF-alpha neutralising activity of each of polypeptides against human TNF-alpha.

Materials

-   -   L929 cells (10000 cells/well)     -   Sterile polypropylene 96-well plates     -   DMEM     -   Human TNF-alpha concentration: 500 pg/ml     -   Actinomycin D concentration: 0.75 ug/mL     -   Purified test polypeptide     -   Range of dilutions of the purified polypeptide (for example):         300 nM-5 pM (1:3 dilutions)     -   Human TNF-alpha dose-response curves: 10 ng/mL-0.5 pg/mL     -   incubation times: 22 h     -   Resazurin cell viability reagent

Method

10000 cells/well in 100 ul are plated on day 0 in 96 wells micro-plates in DMEM complete medium and stored over night at 37 degrees C. and 5% CO₂. On day 1 serial dilutions 1:3 (in DMEM+Act.D+TNF) for each purified variable domain are set up (with volumes sufficient for triplicates for each point) starting from a top concentration of 300 nM.

The following controls are added to the plates:

1. DMEM complete+0.75 ug/mL Actinomycin D

2. DMEM complete+0.75 ug/mL Actinomycin D+0.5 ng/mL of h-TNF-alpha

3. DMEM complete+0.01% Triton (only in the plate containing the TNF-alpha dose responses)

4. DMEM complete (only in the plates containing the TNF-alpha dose responses)

The medium is removed from each well of the microplates and the cells are incubated with 100 ul of each polypeptide dilution or with 100 ul of the different controls. After 22 h of incubation at 37 degrees C. and 5% CO₂, 10 ul of resazurin is added to each well and the cells are incubated for 2 h at 37 degrees C. 50 ul of 3% SDS is subsequently added to each well. The plates are then read using a fluorescent plate reader Ex544 nm/Em590 nm.

Suitably the TNF-alpha binding polypeptide neutralizes human TNF-alpha cytotoxicity in the L929 assay with an EC50 of 100 nM or less, such as 50 nM or less, such as 10 nM or less, such as 5 mM or less, such as 1 nM or less, such as 0.9 nM or less, such as 0.8 nM or less, such as 0.7 nM or less, such as 0.6 nM or less, such as 0.5 nM or less, such as 0.4 nM or less, such as 0.3 nM or less, such as 0.2 nM or less, such as 0.15 nM or less.

The neutralising ability of a TNF-alpha binding polypeptide may also be ascertained by ELISA. Suitably, the TNF-alpha binding polypeptide inhibits binding of human TNF-alpha to TNFR1 in an ELISA assay with an EC50 of 30 nM or less, more suitably 10 nM or less, more suitably 3 nM or less, more suitably 1 nM or less, more suitably 0.6 nM or less, more suitably 0.5 nM or less, more suitably 0.4 nM or less.

Alternatively or in addition, the TNF-alpha binding polypeptide inhibits binding of human TNF-alpha to TNFR2 in an ELISA assay with an EC50 of 2 nM or less, more suitably 1 nM or less, more suitably 0.9 nM or less, more suitably 0.8 nM or less, more suitably 0.7 nM or less, more suitably 0.6 nM or less, more suitably 0.5 nM or less, more suitably 0.4 nM or less.

Structural Properties

Suitably the TNF-alpha binding polypeptide is a polypeptide comprising an antibody fragment. The polypeptide may be an antibody. Suitably the antibody fragment is selected from the group consisting of: V-NARs, scFvs, Fab fragments, F(ab′)2 fragments or immunoglobulin chain variable domains such as VLs, VHHs and VHs. More suitably the antibody fragment is an immunoglobulin chain variable domain, more suitably a VHH or VH, most suitably a VHH.

Suitably the TNF-alpha binding polypeptide comprises three CDRs (CDR1, CDR2 and CDR3).

Suitably CDR1 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence sharing 20% or greater, more suitably 40% or greater, more suitably 60% or greater, more suitably 80% or greater sequence identity with SEQ ID NO: 1.

Alternatively, CDR1 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence having no more than 3, more suitably no more than 2, more suitably no more than 1 addition(s), substitution(s) and/or deletion(s) compared to SEQ ID NO: 1.

Suitably any residues of CDR1 of the TNF-alpha binding polypeptide differing from their corresponding residues in SEQ ID NO: 1 are conservative substitutions with respect to their corresponding residues. Suitably CDR1 comprises or more suitably consists of SEQ ID NO: 1.

Suitably CDR2 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence sharing 20% or greater, more suitably 30% or greater, more suitably 40% or greater, more suitably 50% or greater, more suitably 55% or greater, more suitably 60% or greater, more suitably 70% or greater, more suitably 75% or greater, more suitably 80% or greater, more suitably 85% or greater, more suitably 90% or greater sequence identity, with SEQ ID NO: 2.

Alternatively, CDR2 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence having no more than 8, more suitably no more than 7, more suitably no more than 6, more suitably no more than 5, more suitably no more than 4, more suitably no more than 3, more suitably no more than 2, more suitably no more than 1 addition(s), substitution(s) and/or deletion(s) compared to SEQ ID NO: 2.

Suitably any residues of CDR2 of the TNF-alpha binding polypeptide differing from their corresponding residues in SEQ ID NO: 2 are conservative substitutions with respect to their corresponding residues. Suitably the residue of CDR2 of the TNF-alpha binding polypeptide corresponding to residue number 10 of SEQ ID NO: 2 is R, H, D, E, N, Q, S, T, Y, G, A, V, L, W, P, M, C, F or I (most suitably H). Suitably CDR2 of the TNF-alpha binding polypeptide comprises or more suitably consists of SEQ ID NO: 2.

Suitably CDR3 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence sharing 30%, more suitably 50%, more suitably 60%, more suitably 80% or greater sequence identity with SEQ ID NO: 3.

Alternatively, CDR3 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence having no more than 3, more suitably no more than 2, more suitably no more than 1 addition(s), substitution(s) and/or deletion(s) compared to SEQ ID NO: 3.

Suitably any residues of CDR3 of the TNF-alpha binding polypeptide differing from their corresponding residues in SEQ ID NO: 3 are conservative substitutions with respect to their corresponding residues. Suitably the residue of CDR3 of the TNF-alpha binding polypeptide corresponding to residue number 3 of SEQ ID NO: 3 is R, H, D, E, N, Q, S, T, Y, G, A, V, L, W, P, M, C, F or I; or suitably R, H, D, E, N, Q, S, T, Y, G, V, L, W, P, M, C, F or I (most suitably H). Suitably the residue of CDR3 of the TNF-alpha binding polypeptide corresponding to residue number 3 of SEQ ID NO: 3 is H and any other residues of CDR3 of the TNF-alpha binding polypeptide differing from their corresponding residues in SEQ ID NO: 3 are conservative substitutions with respect to their corresponding residues. Suitably CDR3 of the TNF-alpha binding polypeptide comprises or more suitably consists of SEQ ID NO: 3.

Alternatively CDR3 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence sharing 30%, such as 50%, such as 60%, such as 80% or greater sequence identity with SEQ ID NO: 3 and residue number 3 of CDR3 is R, D, N, C, E, Q, G, H, I, L, K, M, F, P, S, T, W, Y or V (suitably H or a conservative substitution of H; more suitably H). Alternatively residue number 3 of CDR3 is H or a conservative substitution of H (most suitably H) and any other residues of CDR3 differing from their corresponding residues in SEQ ID NO: 3 are conservative substitutions.

Suitably residue 1 of CDR1 of the TNF-alpha binding polypeptide is S, V or N; residues 2 to 4 are HWM and residue 5 is Y or C. Suitably, residues 1 to 9 of CDR2 of the TNF-alpha binding polypeptide are EINTNGLIT; residue 10 is H, K, S or N; residue 11 is Y, residue 12 is G, V, I or A; residue 13 is D; residue 14 is S or F; residue 15 is V or T; residue 16 is H, K, R or G and residue 17 is G. Suitably residue 1 of CDR3 of the TNF-alpha binding polypeptide is N; residue 2 is Q or E; residue 3 is H, K, M or R and residues 4 to 6 are GLN.

Suitably the TNF-alpha binding polypeptide comprises three CDRs (CDR1, CDR2 and CDR3) and four framework regions (FR1-FR4).

Suitably FR1 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence sharing 5%, 12%, 18%, 26%, 32%, 38%, 46%, 52%, 58%, 62%, 66%, 68%, 72%, 75%, 78%, 82%, 85%, 90% or 95% or greater sequence identity, with SEQ ID NO: 4.

Suitably any residues of FR1 of the TNF-alpha binding polypeptide differing from their corresponding residues in SEQ ID NO: 4 are conservative substitutions with respect to their corresponding residues. Suitably the residue of FR1 of the TNF-alpha binding polypeptide corresponding to residue number 1 of SEQ ID NO: 4 is G, A, V, L, I, F, P, S, T, Y, C, M, K, R, H, W, D, E or N (more suitably D or E, most suitably D). Suitably the residue of FR1 of the TNF-alpha binding polypeptide corresponding to residue number 5 of SEQ ID NO: 4 is G, A, V, L, I, F, P, S, T, Y, C, M, K, R, H, W, D, E or N (suitably V). Suitably the residues of FR1 of the TNF-alpha binding polypeptide corresponding to residue numbers 1 to 5 of SEQ ID NO: 4 are DVQLV. Suitably the residue of FR1 of the TNF-alpha binding polypeptide corresponding to residue numbers 20 and/or 24 of SEQ ID NO: 4 are an amino acid which is hydrophobic (most suitably L or A, respectively). Suitably the residue of FR1 of the TNF-alpha binding polypeptide corresponding to residue number 29 of SEQ ID NO: 4 is F. Suitably FR1 of the TNF-alpha binding polypeptide comprises or more suitably consists of SEQ ID NO: 4.

Suitably FR2 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence sharing 10%, 15%, 25%, 30%, 40%, 45%, 55%, 60%, 70%, 75%, 85% or 90% or greater sequence identity, with SEQ ID NO: 5.

Suitably any residues of FR2 of the TNF-alpha binding polypeptide differing from their corresponding residues in SEQ ID NO: 5 are conservative substitutions with respect to their corresponding residues. Suitably the residues of FR2 of the TNF-alpha binding polypeptide corresponding to residue numbers 8 to 11 of SEQ ID NO: 5 are KEXE, wherein X is R or L. Alternatively the residues of FR2 of the TNF-alpha binding polypeptide corresponding to residue numbers 9 to 12 of SEQ ID NO: 5 are GLEW. Suitably FR2 of the TNF-alpha binding polypeptide comprises or more suitably consists of SEQ ID NO: 5.

Suitably FR3 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence sharing 8%, 15%, 20%, 26%, 32%, 40%, 45%, 52%, 58%, 65%, 70%, 76%, 80%, 82%, 85%, 90%, 92% or 95% or greater sequence identity, with SEQ ID NO: 6.

Suitably the residue of FR3 of the TNF-alpha binding polypeptide corresponding to residue number 26 of SEQ ID NO: 6 is an amino acid which is hydrophobic (suitably A). Suitably any residues of FR3 of the TNF-alpha binding polypeptide differing from their corresponding residues in SEQ ID NO: 6 are conservative substitutions with respect to their corresponding residues. Suitably FR3 of the TNF-alpha binding polypeptide comprises or more suitably consists of SEQ ID NO: 6.

Suitably FR4 of the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence sharing 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 90% or greater sequence identity, with SEQ ID NO: 7.

Suitably any residues of FR4 of the TNF-alpha binding polypeptide differing from their corresponding residues in SEQ ID NO: 7 are conservative substitutions with respect to their corresponding residues. Suitably FR4 of the TNF-alpha binding polypeptide comprises or more suitably consists of SEQ ID NO: 7.

Suitably the TNF-alpha binding polypeptide comprises or more suitably consists of a sequence sharing 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% or greater sequence identity, with SEQ ID NO: 8. Suitably the N-terminus of the TNF-alpha binding polypeptide is D. Suitably the TNF-alpha binding polypeptide comprises or more suitably consists of SEQ ID NO: 8.

According to a specific embodiment, the TNF-alpha binding polypeptide has an amino acid sequence which is not exactly the same as (i.e. shares 100% sequence identity with) the amino acid sequence of a naturally occurring polypeptide.

IL-6R Binding Polypeptides

Functional Properties

An anti-IL-6R polypeptide, a polypeptide which interacts with IL-6R, or a polypeptide against IL-6R, are all effectively IL-6R binding polypeptides. An IL-6R binding polypeptide may bind to a linear or conformational epitope on IL-6R. The term “binds to IL-6R” means binding to IL-6R wherein, for example, IL-6R may be comprised within the IL-6 receptor complex wherein the IL-6R receptor comprises gp130 and/or IL-6.

Suitably, the IL-6R binding polypeptide will bind to both soluble and membrane IL-6R and more suitably with higher affinity to soluble IL-6R than membrane IL-6R. Suitably, the IL-6R binding polypeptide will bind to human IL-6R.

Suitably the IL-6R binding polypeptide is directed against epitopes on IL-6R (and in particular epitopes on IL-6R which are exposed when IL-6R is comprised in an IL-6/IL-6R complex) that lie in and/or form part of the gp130-binding site(s) of the IL-6/IL-6R complex, such that said polypeptide, upon binding to IL-6R, results in inhibiting or reducing signalling mediated by the IL-6/IL-6R complex via gp130 association.

Suitably, the IL-6R binding polypeptide binds to IL-6R with an equilibrium dissociation constant (Kd) of 10⁻⁶ M or less, more suitably 10⁻⁷ M or less, more suitably 10⁻⁸ M or less and more suitably 10⁻⁹ M or less.

Suitably, the affinity of the IL-6R binding polypeptide is determined by surface plasmon resonance.

In one embodiment, the affinity of the IL-6R-binding polypeptide is established at 25° C. by amine coupling human IL-6R at 10 ug/mL in a pH 5, 10 mM Sodium acetate buffer to a sensor chip, before exposing the IL-6R binding peptide at five different concentrations between 100 nM and 500 nM in pH 7.4, 0.01 M HEPES, 0.15 M NaCl, 0.05% polysorbate 20 and 3 mM EDTA buffer and a flow rate of 45 uL/min to the chip-bound IL-6R for 3 mins and then observing dissociation for 10 mins by surface plasmon resonance, wherein the bound-IL-6R is regenerated between cycles with 10 mM Glycine, pH 1.5 for 30 seconds.

Suitably the IL-6R binding polypeptide neutralises IL-6R. A neutralising polypeptide for the purposes of the invention is a polypeptide which interferes in the binding of a sIL-6/IL-6R complex to gp130 as measured by ELISA. Alternatively, or in addition, a neutralising polypeptide for the purposes of the invention is a polypeptide which reduces the proliferation of cells presenting surface IL-6R (such as TF-1 cells) which are exposed to exogenous IL-6, by preventing formation of IL-6/IL-6R/gp130 cis-signalling complexes.

Methods for determining the neutralising capability of an IL-6R binding polypeptide are as follows.

1. Standard gp130 ELISA Assay

A method for determining the potency of an anti-IL-6R polypeptide in neutralising IL-6R is as follows.

The objective of this assay is to measure the potency of anti-IL-6R polypeptides by measuring interference in the binding to gp130 of a sIL-6/IL-6R complex. This assay detects binding of hIL-6R/hIL-6 complexes to recombinant human gp130. This interaction can be competitively inhibited by anti-IL-6R polypeptides, causing reduced binding of hIL-6R-hIL-6 complexes to gp130. Therefore, high signal in this ELISA represents a low concentration or low affinity of anti-IL-6R polypeptide, and vice versa. The details below refer to ICVDs but are equally applicable to any IL-6R binding polypeptide.

Materials

Solutions Required:

1×PBS

PBST (1×PBS, 0.05% Tween 20)

Block buffer (1% BSA in 1×PBS, pH 7.3-7.5)

0.5 M Sulphuric acid (H₂SO₄)

Reagents Required:

Recombinant soluble human gp130 at known concentration

ICVD stock of known concentration

Recombinant soluble human IL-6 at known concentration

Recombinant soluble human IL-6R at known concentration

Biotinylated goat anti-IL-6R polyclonal antibody (R&D systems BAF227); resuspended at 250 ug/ml in sterile PBS.

ExtrAvidin-Peroxidase (Sigma E2886)

TMB substrate (Microwell Peroxidase substrate System 2-C, KPL, 50-70-00)

Procedure

Preparation:

-   -   1. Determine number of plates required for the assay.     -   2. Prepare the relevant volume (up to 3 plates at a time) of 0.2         μg/ml recombinant soluble human gp130 in PBS with 5 ug/mL BSA in         1×PBS.     -   3. Working quickly, dispense 50 μl/well into Max isorp 96-well         ELISA plates (Nunc), loading a maximum of 3 plates in one batch.     -   4. Shake plate briefly, seal and incubate at 4° C. overnight.

Assay:

1. Wash the ELISA plate using a plate washer (4×-380 μl PBST). Bang the plate on towel to remove residual liquid.

2. Apply 200 μl/well block buffer. Seal and incubate on a rotary plate shaker for ≥1 hour.

3. Prepare a dilution series of ICVD standards between 0.004 nM to 80 nM in minimum final volumes of 70 μl using block buffer as a diluent.

4. Prepare appropriate dilutions of samples to be tested in block buffer, such that their estimated final concentration on the plate will fall in the range of 0.001 nM to 250 nM ICVD.

5. Prepare a 40 ng/ml IL-6R solution in block buffer.

6. In a separate 96-well plate, mix together 50 μl of each ICVD dilution with 50 μl IL-6R solution. In each dilution series include one well with no ICVD. Incubate for 1 hour on a rotary plate shaker.

7. Prepare a 100 ng/ml IL-6 solution in block buffer.

8. In a further additional 96-well plate, mix together 85 μl ICVD-IL-6R mixture from step 6 with 85 μl IL-6 solution prepared in step 7. Include wells containing block buffer only, such that the following controls are applied to each plate: IL-6 only, and no ICVD (IL6+IL6R only). Incubate for 10 minutes on rotary plate shaker.

9. Wash blocked ELISA plate as in step 1.

10. Transfer 50 μl of the mixtures prepared in step 8 to the washed ELISA plate in triplicate.

Seal and incubate on a rotary plate shaker for 2 hours.

11. Wash blocked ELISA plate as in step 1.

12. Prepare 5.2 ml/plate 125 ug/mL of BAF227 anti-hIL-6R antibody made up in block buffer. Add 50 μl/well, seal, shake briefly, and incubate for 1 hour at room temperature or overnight at 4° C.

13. Wash blocked ELISA plate as in step 1.

14. Prepare 5.2 ml/plate of 1/1,000-1/3000 dilution of Extravidin in block buffer. Add 50 μl/well, seal, and incubate on a rotary shaker for 30 mins.

15. Wash blocked ELISA plate as in step 1.

16. Prepare 10 ml/plate TMB substrate (1:1 ratio of substrate A and B). Add 100 μl/well, seal and incubate on a rotary plate shaker until a mid blue colour evolves in the lowest dilution wells or up to a maximum of 30 mins. Shield from light.

17. Stop reaction with 50 μl/well 0.5 M H₂SO₄.

18. Read plate at 450 nm.

19. Use standard curve to interpolate concentrations of active ICVD. Raw OD450 values are adjusted with readings taken from blank control wells. Standard curves are plotted using appropriate software (e.g. Graphpad Prism using Log(inhibitor) vs. response-variable slope (four parameters)). ICVD concentrations in the test samples are calculated in the software using the standard curve.

2. The Standard TF1 Cell Assay

A method for determining the potency of an anti-IL-6R agent in inhibiting membrane bound IL-6R mediated IL-6 cis-signalling is as follows. This assay detects the activity of exogenous IL-6 on TF1 cell proliferation. TF1 cells are a human erythroblast immortal cell line that expresses the membrane-bound IL-6 receptor on their surface. In the presence of exogenously added IL-6, the cells are stimulated via the IL-6 cis-signalling pathway to proliferate. Anti-membrane-bound IL-6R compounds prevent the formation of the complete IL-6/IL-6R/gp130 complex that is required for signalling, reducing IL-6-stimulated proliferation in dose-dependent manner. Cell proliferation is measured after two days using resazurin, a blue dye that is irreversibly reduced to the pink coloured and highly red fluorescent resorufin by cellular metabolic processes. Details below refer to ICVDs or antibodies but are equally applicable to any IL-6R binding polypeptide.

Materials

Standard Components:

Cell line: TF-1 (Public Health England, Cat. No. 93022307). Exponentially growing cells (<5×10{circumflex over ( )}5 cells/mL) cultivated in Advanced RPMI with 5% heat-inactivated foetal bovine serum and 2.5 ng/mL GM-CSF (Human Granulocyte Macrophage Colony Stimulating Factor).

Assay medium: Advanced RMPI (LifeTech 12633-012) with 2 mM L-glutamine, Pen/Strep

1×PBS

3% SDS

Sterile MQ water

Sterile 96 well micro-titre plates for cell culture, flat bottomed, optically clear

12 multi-channel pipette and filtered tips

Reagents:

Recombinant soluble human IL-6 at known concentration

Anti-IL-6R antibodies or ICVD of known concentration

Resazurin (Alamar Blue; LifeTech, DAL1100)

Procedure

Cell Preparation:

-   -   a. Pre-warm media and 1×PBS in a 37° C. water bath.     -   b. Determine the number of plates required for the assay.     -   c. Fill the outside wells with 320 uL of sterile MilliQ water.     -   d. Fill the spaces between the wells with 160 uL of the same         water.     -   e. Calculate the volume of the cell culture you will need to         have 20,000 cells/well using the equation:

$\frac{\begin{matrix} {60\mspace{14mu} {wells}\mspace{14mu} {per}\mspace{14mu} {plate} \times \# \mspace{14mu} {plates} \times 20,000\mspace{14mu} {cells}\text{/}{well} \times} \\ {1.2\mspace{14mu} \left( {{for}\mspace{14mu} 20\% \mspace{14mu} {overage}} \right)} \end{matrix}}{{Cell}\mspace{14mu} {count}\mspace{14mu} \left( {{cells}\text{/}{ml}} \right)} = {{total}\mspace{14mu} {cells}}$

-   -   f. Transfer cells to falcon tube. Take to maximum tube volume         with 1×PBS. Spin 5′ at 1.1 k×rpm at 20 degrees C.     -   g. Remove medium from cell pellet with a 10 mL stripette, leave         ˜200 uL on the cells, ensuring no cells are aspirated. Tap cells         in residual volume to resuspend.     -   h. Wash cells in full tube volume of 1×PBS spin as before.     -   i. Remove 1×PBS with a 10 mL stripette, leave ˜200 uL on the         cells, ensuring no cells are aspirated. Remove residual with         P200.     -   j. Resuspend cell pellet by tapping then add assay medium using         the equation below to calculate the volume required:

60 wells per plate×# plates×0.05 mL volume per well×1.2 (for 20% overage)=total volume

-   -   k. Fill plates with 50 ul cells per well proceeding row by row.         Place filled plates in the incubator. Agitate the cells by         pipetting or shaking the trough intermittently during this         process.

ICVD/Antibody Preparation:

-   -   a. Prepare the assay stock of IL-6 at 20 ng/mL (4× the assay         concentration) in a volume of assay medium sufficient to add 25         ul per well.     -   b. Prepare a 9 point serial dilution series of ICVD reference         standards at 4× the assay concentration (being between 0.04 nM         and 2500 nM in minimum final volumes of 100 μl using assay         medium as a diluent. In a tenth well, add assay medium only. For         example, starting in well A1 make the dilutions series along to         plate to well A9. In well A10, add medium only.     -   c. In a fresh microtitre plate, add a minimum volume of 85 uL of         IL-6 to the equivalent 9 wells used in the dilution series. In         the tenth well add either assay medium or IL-6 to the effect         that each final assay plate will have wells with IL-6 only         (maximum proliferation) and media only (minimum proliferation).     -   d. To the IL-6 mix plate prepared above, add an equivalent         volume (e.g. 85 uL) of each ICVD/antibody serial dilution. At         this stage both IL-6 and ICVD will be at 2× the assay         concentration.

Assay:

-   -   a. Mix the ICVD/Antibody & IL-6 mixtures by pipetting and add 50         ul of each mix to the cells.     -   b. Incubate the cells for 2 days at 37° C., 5% CO₂.     -   c. Add 10 uL of AlamarBlue to cells. Protect from light.     -   d. Shake the cells gently for 30 s on a plate shaker to mix     -   e. Incubate 37° C., 5% CO₂ for 2 hours.     -   f. Stop cellular processes with 50 uL 3% SDS. Protect from light     -   g. Read on plate reader (e.g. BMG Fluorstar) at Ex 544 nm-Em 590         nm     -   h. Use calibration curve to interpolate unknown sample         concentrations. Raw OD450 values are adjusted with readings         taken from blank control wells. Standard curves are plotted         using appropriate software (e.g. Graphpad Prism using         Log(inhibitor) vs. response —variable slope (four parameters)).         ICVD concentrations in the test samples are calculated in the         software using the standard curve.

The M1 Cell Assay

The M1 cell assay may be used to investigate the IL-6 trans-signalling neutralising potency of polypeptides specific for IL-6R. M1 cells respond to exogenous IL-6+IL-6R by inhibition of proliferation, by differentiation and eventually cell death, but this response can be negated by IL-6R specific polypeptides that prevent IL-6R-IL-6 binding. The discussion below refers to ICVDs but is equally applicable to any IL-6R binding polypeptide.

The M1 assay measures the effect, in terms of cell behaviour, of ICVD blockade of IL-6 trans-signalling over a period of days. In assessment of ICVD trans selectivity, the TF-1 cell assay is used to measure cis IL-6 signalling; it is therefore appropriate when determining the degree of trans vs cis selectivity, to use data from another cellular assay, dependent on IL-6 trans signalling, such as the M1 cell assay, for comparison. Details are provided in respect of ICVDs but these methods are equally applicable to any IL-6R binding polypeptide.

M1 cells from a rapidly growing stock culture are inoculated into 96-well assay plates in RPMI medium+3% FCS at 5×10⁴ cells/50 μl/well. IL-6, IL-6R and concentration ranges of ICVDs are all prepared in the same medium at 6× the final assay concentration (20 ng/ml IL-6R, 100 ng/ml IL-6). 75 μl of each ICVD dilution is mixed with the same volume of 120 ng/ml IL-6R and incubated for 1 hour at room temperature, before addition of 75 μl of 600 ng/ml IL-6 to each of these mixtures. Finally, 50 μl of each ICVD/IL-6R/IL-6 mixture is added to four replicate wells of M1 cells, and the plates incubated undisturbed for 5 days. Viable cell mass is then measured by Alamar blue addition (10 μl/well), further incubated for 5 hours, and finally 50 μl 3% SDS solution is added, and fluorescence measured at 620 nm. IL-6 only and IL-6+IL-6R only controls represent 0% and 100% of the IL-6+IL-6R stimulated response.

Suitably the IL-6R binding polypeptide neutralizes sIL-6R-IL-6 binding to gp130 in an ELISA assay such as the standard gp130 ELISA with an EC50 of 100 nM or less, such as 75 nM or less, such as 50 nM or less, such as 40 nM or less, such as 30 nM or less, such as 25 nM or less, such as 20 nM or less, such as 10 nM or less, such as 5 nM or less, such as 2 nM or less, such as 1.5 nM or less, such as 1 nM or less, such as 0.9 nM or less, such as 0.8 nM or less, such as 0.7 nM or less, such as 0.6 nM or less, such as 0.5 nM or less.

Suitably the IL-6R binding polypeptide prevents proliferation of TF-1 cells in the standard TF-1 assay with an EC50 of 20 nM or less, such as 15 nM or less, such as 10 nM or less, such as 6 nM or less, such as 5 nM or less, such as 4.5 nM or less.

Suitably the IL-6R binding polypeptide prevents proliferation of M1 cells in the M1 cell assay with an EC₅₀ of 20 nM or less, such as 15 nM or less, such as 10 nM or less, such as 6 nM or less, such as 5 nM or less, such as 4.5 nM or less.

Suitably the IL-6R binding polypeptide inhibits IL-6R trans-signalling to a higher extent than it inhibits IL-6R cis-signalling, i.e. the polypeptide is ‘trans-selective’.

Structural Properties

Suitably the IL-6R binding polypeptide is a polypeptide comprising an antibody fragment. The polypeptide may be an antibody. Suitably the antibody fragment is selected from the group consisting of: V-NARs, scFvs, Fab fragments, F(ab′)2 fragments or immunoglobulin chain variable domains such as VLs, VHHs and VHs. More suitably the antibody fragment is an immunoglobulin chain variable domain, more suitably a VHH or VH, most suitably a VHH.

Suitably the IL-6R binding polypeptide comprises three CDRs (CDR1, CDR2 and CDR3).

Suitably CDR1 of the IL-6R binding polypeptide comprises or more suitably consists of a sequence sharing 20%, 40%, 60%, or 80% or greater sequence identity, with SEQ ID NO: 9.

Alternatively, CDR1 of the polypeptide of the IL-6R binding polypeptide comprises or more suitably consists of a sequence having no more than 4, more suitably no more than 3, more suitably no more than 2, more suitably no more than 1 addition(s), substitution(s) and/or deletion(s) compared to SEQ ID NO: 9.

Suitably any residues of CDR1 of the IL-6R binding polypeptide differing from their corresponding residues in SEQ ID NO: 9 are conservative substitutions with respect to their corresponding residues. Suitably CDR1 of the IL-6R binding polypeptide comprises or more suitably consists of SEQ ID NO: 9.

Suitably CDR2 of the IL-6R binding polypeptide comprises or more suitably consists of a sequence sharing 20% or greater, more suitably 30% or greater, more suitably 40% or greater, more suitably 50% or greater, more suitably 55% or greater, more suitably 60% or greater, more suitably 65% or greater, more suitably 70% or greater, more suitably 75% or greater, more suitably 80% or greater, more suitably 85% or greater, more suitably 90% or greater sequence identity, with SEQ ID NO: 10.

Alternatively, CDR2 of the IL-6R binding polypeptide comprises or more suitably consists of a sequence having no more than 8, more suitably no more than 7, more suitably no more than 6, more suitably no more than 5, more suitably no more than 4, more suitably no more than 3, more suitably no more than 2, more suitably no more than 1 addition(s), substitution(s) and/or deletion(s) compared to SEQ ID NO: 10.

Suitably any residues of CDR2 of the IL-6R binding polypeptide differing from their corresponding residues in SEQ ID NO: 10 are conservative substitutions with respect to their corresponding residues. Suitably CDR2 of the IL-6R binding polypeptide comprises or more suitably consists of SEQ ID NO: 10.

Suitably CDR3 of the IL-6R binding polypeptide comprises or more suitably consists of a sequence sharing 20% or greater, more suitably 30% or greater, more suitably 40% or greater, more suitably 50% or greater, more suitably 55% or greater, more suitably 60% or greater, more suitably 65% or greater, more suitably 70% or greater, more suitably 75% or greater, more suitably 80% or greater, more suitably 85% or greater, more suitably 90% or greater sequence identity with SEQ ID NO: 11.

Alternatively, CDR3 of the IL-6R binding polypeptide comprises or more suitably consists of a sequence having no more than 6, more suitably no more than 5, more suitably no more than 4, more suitably no more than 3, more suitably no more than 2, more suitably no more than 1 addition(s), substitution(s) and/or deletion(s) compared to SEQ ID NO: 11.

Suitably any residues of CDR3 of the IL-6R binding polypeptide differing from their corresponding residues in SEQ ID NO: 11 are conservative substitutions with respect to their corresponding residues.

Suitably the residue of CDR3 of the IL-6R binding polypeptide corresponding to residue number 5 of SEQ ID NO: 11 is R or H, most suitably H. Suitably the residue of CDR3 of the IL-6R binding polypeptide corresponding to residue number 5 of SEQ ID NO: 11 is R or H, most suitably H, and any other residues of CDR3 of the IL-6R binding polypeptide differing from their corresponding residues in SEQ ID NO: 11 are conservative substitutions with respect to their corresponding residues.

Suitably the residue of CDR3 of the IL-6R binding polypeptide corresponding to residue number 9 of SEQ ID NO: 11 is F, L or H, more suitably F or H, most suitably H. Suitably the residue of CDR3 of the IL-6R binding polypeptide corresponding to residue number 9 of SEQ ID NO: 11 is F, L or H, most suitably H, and any other residues of CDR3 differing from their corresponding residues in SEQ ID NO: 11 are conservative substitutions with respect to their corresponding residues.

Suitably the residue of CDR3 of the IL-6R binding polypeptide corresponding to residue number 11 of SEQ ID NO: 11 is A, G, or a conservative substitution thereof. Suitably the residue of CDR3 of the IL-6R binding polypeptide corresponding to residue number 11 of SEQ ID NO: 11 is A or G, most suitably A. Suitably the residue of CDR3 of the IL-6R binding polypeptide corresponding to residue number 11 of SEQ ID NO: 11 is A or G, most suitably A, and any other residues of CDR3 differing from their corresponding residues in SEQ ID NO: 11 are conservative substitutions with respect to their corresponding residues.

Suitably CDR3 of the IL-6R binding polypeptide comprises or more suitably consists of SEQ ID NO: 11.

Suitably the IL-6R binding polypeptide comprises three CDRs (CDR1, CDR2 and CDR3) and four framework regions (FR1-FR4).

Suitably FR1 of the IL-6R binding polypeptide comprises or more suitably consists of a sequence sharing 5%, 12%, 18%, 26%, 32%, 38%, 46%, 52%, 58%, 62%, 66%, 68%, 72%, 75%, 78%, 82%, 85%, 90% or 95% or greater sequence identity, with SEQ ID NO: 12.

Suitably any residues of FR1 of the IL-6R binding polypeptide differing from their corresponding residues in SEQ ID NO: 12 are conservative substitutions with respect to their corresponding residues.

Suitably the residue of FR1 of the IL-6R binding polypeptide corresponding to residue number 1 of SEQ ID NO: 12 is G, A, V, L, I, F, P, S, T, Y, C, M, K, R, H, W, D, E or N (more suitably D or E, most suitably D). Suitably the residue of FR1 of the IL-6R binding polypeptide corresponding to residue number 23 of SEQ ID NO: 12 is K or L. Suitably the residues of FR1 of the IL-6R binding polypeptide corresponding to residue numbers 2 to 5 of SEQ ID NO: 12 are VQLV. Suitably the residue of FR1 of the IL-6R binding polypeptide corresponding to residue number 29 of SEQ ID NO: 12 is F or S, most suitably S. Suitably the residue of FR1 of the IL-6R binding polypeptide corresponding to residue number 30 of SEQ ID NO: 12 is N or S. Suitably FR1 of the IL-6R binding polypeptide comprises or more suitably consists of SEQ ID NO: 12.

Suitably FR1 of the IL-6R binding polypeptide comprises the sequence NIN or three consecutive amino acids wherein one or more of the amino acids is a conservative substitution of the corresponding amino acid in the sequence NIN. Most suitably FR1 of the IL-6R binding polypeptide comprises the sequence NIN. More suitably the last four C-terminal residues of FR1 of the IL-6R binding polypeptide are NINX or four consecutive amino acids wherein one or more of the amino acids is a conservative substitution of the corresponding amino acid in the sequence NINX, wherein X is any amino acid. Suitably X is S or a conservative substitution of S, most suitably X is S. More suitably FR1 of the IL-6R binding polypeptide consists of 33 residues and the last four residues of FR1 are NINS.

Suitably FR2 of the IL-6R binding polypeptide comprises or more suitably consists of a sequence sharing 10%, 15%, 25%, 30%, 40%, 45%, 55%, 60%, 70%, 75%, 85% or 90% or greater sequence identity, with SEQ ID NO: 13.

Suitably any residues of FR2 of the IL-6R binding polypeptide differing from their corresponding residues in SEQ ID NO: 13 are conservative substitutions with respect to their corresponding residues. Suitably the residue of FR2 of the IL-6R binding polypeptide corresponding to residue number 9 of SEQ ID NO: 13 is G or Q. Suitably the residues of FR2 of the IL-6R binding polypeptide corresponding to residue numbers 8 to 11 of SEQ ID NO: 13 are KERE, KELE, KGRE or KQRE; most suitably KGRE or KQRE. Suitably FR2 of the IL-6R binding polypeptide comprises or more suitably consists of SEQ ID NO: 13.

Suitably FR3 of the IL-6R binding polypeptide comprises or more suitably consists of a sequence sharing 8%, 15%, 20%, 26%, 32%, 40%, 45%, 52%, 58%, 65%, 70%, 76%, 80%, 82%, 85%, 90%, 92% or 95% or greater sequence identity, with SEQ ID NO: 14.

Suitably the residue of FR3 of the IL-6R binding polypeptide corresponding to residue number 8 of SEQ ID NO: 14 is an amino acid which is hydrophobic (suitably A or N, more suitably A). Suitably the residue of FR3 of the IL-6R binding polypeptide corresponding to residue number 9 of SEQ ID NO: 14 is an amino acid which is hydrophobic (suitably A or S, more suitably A). Suitably the residue of FR3 of the IL-6R binding polypeptide corresponding to residue number 13 of SEQ ID NO: 14 is V or L, most suitably V. Suitably the residue of FR3 of the IL-6R binding polypeptide corresponding to residue number 14 of SEQ ID NO: 14 is N or Y, most suitably Y. Suitably the residue of FR3 of the IL-6R binding polypeptide corresponding to residue number 21 of SEQ ID NO: 14 is R or K, most suitably R.

Suitably any residues of FR3 differing from their corresponding residues in SEQ ID NO: 14 are conservative substitutions with respect to their corresponding residues. Suitably FR3 comprises or more suitably consists of SEQ ID NO: 14.

Suitably FR4 of the IL-6R binding polypeptide comprises or more suitably consists of a sequence sharing 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 90% or greater sequence identity, with SEQ ID NO: 15.

Suitably any residues of FR4 of the IL-6R binding polypeptide differing from their corresponding residues in SEQ ID NO: 15 are conservative substitutions with respect to their corresponding residues. Suitably FR4 of the IL-6R binding polypeptide comprises or more suitably consists of SEQ ID NO: 15.

Suitably the IL-6R binding polypeptide comprises or more suitably consists of a sequence sharing 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% or greater sequence identity, with SEQ ID NO: 16.

Suitably the N-terminus of the IL-6R binding polypeptide is D. Suitably the IL-6R binding polypeptide comprises or more suitably consists of SEQ ID NO: 16.

According to a specific embodiment, the IL-6R binding polypeptide has an amino acid sequence which is not exactly the same as (i.e. shares 100% sequence identity with) the amino acid sequence of a naturally occurring polypeptide.

Particular Combined Structural and Functional Properties of Both the TNF-Alpha Binding Polypeptide and the IL-6R Binding Polypeptide

Suitably both the TNF-alpha binding polypeptide and the IL-6R binding polypeptide are immunoglobulin chain variable domains wherein:

(a) CDR1 of the TNF-alpha binding polypeptide comprises a sequence sharing 40% or greater sequence identity with SEQ ID NO: 1;

(b) CDR2 of the TNF-alpha binding polypeptide comprises a sequence sharing 40% or greater sequence identity with SEQ ID NO: 2;

(c) CDR3 of the TNF-alpha binding polypeptide comprises a sequence sharing 50% or greater sequence identity with SEQ ID NO: 3;

(d) CDR1 of the IL-6R binding polypeptide comprises a sequence sharing 40% or greater sequence identity with SEQ ID NO: 9;

(e) CDR2 of the IL-6R binding polypeptide comprises a sequence sharing 40% or greater sequence identity with SEQ ID NO: 10;

(f) CDR3 of the IL-6R binding polypeptide comprises a sequence sharing 50% or greater sequence identity with SEQ ID NO: 11, more suitably wherein:

(a) CDR1 of the TNF-alpha binding polypeptide comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO: 1;

(b) CDR2 of the TNF-alpha binding polypeptide comprises a sequence sharing 50% or greater sequence identity with SEQ ID NO: 2;

(c) CDR3 of the TNF-alpha binding polypeptide comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO: 3;

(d) CDR1 of the IL-6R binding polypeptide comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO: 9;

(e) CDR2 of the IL-6R binding polypeptide comprises a sequence sharing 50% or greater sequence identity with SEQ ID NO: 10;

(f) CDR3 of the IL-6R binding polypeptide comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO: 11, more suitably wherein:

(a) CDR1 of the TNF-alpha binding polypeptide comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO: 1;

(b) CDR2 of the TNF-alpha binding polypeptide comprises a sequence sharing 70% or greater sequence identity with SEQ ID NO: 2;

(c) CDR3 of the TNF-alpha binding polypeptide comprises a sequence sharing 65% or greater sequence identity with SEQ ID NO: 3;

(d) CDR1 of the IL-6R binding polypeptide comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO: 9;

(e) CDR2 of the IL-6R binding polypeptide comprises a sequence sharing 70% or greater sequence identity with SEQ ID NO: 10;

(f) CDR3 of the IL-6R binding polypeptide comprises a sequence sharing 65% or greater sequence identity with SEQ ID NO: 11, more suitably wherein:

(a) CDR1 of the TNF-alpha binding polypeptide comprises a sequence sharing 80% or greater sequence identity with SEQ ID NO: 1;

(b) CDR2 of the TNF-alpha binding polypeptide comprises a sequence sharing 85% or greater sequence identity with SEQ ID NO: 2;

(c) CDR3 of the TNF-alpha binding polypeptide comprises a sequence sharing 80% or greater sequence identity with SEQ ID NO: 3;

(d) CDR1 of the IL-6R binding polypeptide comprises a sequence sharing 80% or greater sequence identity with SEQ ID NO: 9;

(e) CDR2 of the IL-6R binding polypeptide comprises a sequence sharing 85% or greater sequence identity with SEQ ID NO: 10;

(f) CDR3 of the IL-6R binding polypeptide comprises a sequence sharing 80% or greater sequence identity with SEQ ID NO: 11,

and in each case wherein most suitably the TNF-alpha binding polypeptide neutralizes human TNF-alpha cytotoxicity in the L929 assay with an EC50 of 100 nM or less and the IL-6R binding polypeptide neutralizes sIL-6R-IL-6 binding to gp130 in the standard gp130 ELISA with an EC50 of 100 nM or less; and/or wherein the TNF-alpha binding polypeptide binds to TNF-alpha with a Kd of 10⁻⁷ M or less and the IL-6R binding polypeptide binds to IL-6R with a Kd of 10⁻⁷ M or less.

Format of TNF-Alpha and IL-6R Binding Polypeptides

The TNF-alpha binding polypeptide and the IL-6R binding polypeptide may be linked or unlinked.

In one embodiment, the TNF-alpha binding polypeptide and the IL-6R binding polypeptide may be present in the composition of the invention independently from one another (i.e. the TNF-alpha and IL-6R binding polypeptides are not linked to each other). In a specific embodiment, the composition comprises (a) ID-38F (SEQ ID NO: 8) or a polypeptide having at least 75%, more suitably at least 85% identity thereto and (b) ID-142V (SEQ ID NO: 16) or a polypeptide having at least 75%, more suitably at least 85% identity thereto.

In a further embodiment, the TNF-alpha binding polypeptide and the IL-6R binding polypeptide comprised in the composition of the invention are linked to eachother (thereby forming a single construct). Such a format may be convenient for recombinant expression purposes. Such a construct of the invention is therefore multimeric and multivalent. If no further polypeptides are comprised within the construct, then such a construct may be referred to as a ‘heterobihead’. A multivalent construct comprises two or more binding polypeptides and therefore provides two or more sites at which attachment to antigens can occur (suitably before or after cleavage of the labile peptide linker, if such a linker is present in the construct—see ‘Linkers’ below).

A construct of the invention may comprise an additional third polypeptide (connected to the TNF-alpha or IL-6R binding polypeptide directly or by a linker) and may also comprise or consist of an additional fourth polypeptide (connected to the TNF-alpha or IL-6R binding polypeptide directly or by a linker). A construct of the invention consisting of four polypeptides is known as a ‘quadrahead’. A quadrahead may for example have the format anti-TNF-alpha-anti-IL-6R-anti-IL-6R-anti-TNF-alpha, anti-TNF-alpha-anti-IL-6R-anti-TNF-alpha-anti-IL-6R or anti-IL-6R-anti-TNF-alpha-anti-TNF-alpha-anti-IL6R. The linkers between these binding polypeptides may be labile or non-labile (see below under ‘Linkers’). For example, a quadrahead may for example have the format anti-TNF-alpha-anti-IL-6R-(labile linker)-anti-IL-6R-anti-TNF-alpha, anti-TNF-alpha-(labile linker)-anti-IL-6R-anti-IL-6R-(labile linker)-anti-TNF-alpha or anti-IL-6R-(labile linker)-anti-TNF-alpha-anti-TNF-alpha-(labile linker)-anti-IL-6R.

Suitably each polypeptide in the construct has a molecular weight of no greater than 300 kDa, such as 250 kDa, such as 200 kDa, such as 180 kDa, such as 160 kDa, such as 140 kDa, such as 120 kDa, such as 100 kDa, such as 80 kDa, such as 60 kDa.

Linkers

The TNF-alpha and IL-6R binding polypeptides, if linked, can be linked to each other directly (i.e. without use of a linker) or via a linker. Suitably a linker is used. The linker may be a protease-labile or a non-protease-labile linker. The linker is suitably a peptide and suitably will be selected so as to allow binding of the polypeptides to their epitopes. Suitably the linker is flexible, for example sufficiently flexible to allow both binding polypeptides to bind their targets simultaneously (such as a [-(G₄S)—]₄. If used for therapeutic purposes, the linker is suitably non-immunogenic in the subject to which the polypeptides are administered. Suitably the polypeptides and linker are expressed as a single contiguous polypeptide construct.

Suitably the peptide linker has a length of at least 3, such as at least 4, such as at least 5, such as at least 6, such as at least 7, such as at least 8, such as at least 9, such as at least 10 residues. Suitably the peptide linker has a length of no greater than 40, such as no greater than 35, such as no greater than 30, such as no greater than 25, such as no greater than 20, such as no greater than 15 residues.

Suitably the peptide linker consists of any amino acids selected from the list consisting of: arginine, histidine, lysine, aspartic acid, glutamic acid, serine, threonine, asparagine, glutamine, cysteine, glycine, proline, alanine, valine, isoleucine, leucine, methionine, phenylalanine, tyrosine and tryptophan. Proline may be a sub-optimal amino acid for inclusion in a linker and therefore more suitably the peptide linker consists of any amino acids selected from the list consisting of: arginine, histidine, lysine, aspartic acid, glutamic acid, serine, threonine, asparagine, glutamine, cysteine, glycine, alanine, valine, isoleucine, leucine, methionine, phenylalanine, tyrosine and tryptophan.

The TNF-alpha and IL-6R binding polypeptides, if linked, may be in the orientation (from N- to C-terminus) anti-TNF-alpha-linker-anti-IL-6R or may be in the orientation anti-IL6R-linker-anti-TNF-alpha. Most suitably, they are in the orientation anti-TNF-alpha-linker-anti-IL-6R.

Compositions of the invention comprising TNF-alpha and IL-6R binding polypeptides linked by peptide linkers may for example be obtained by preparing a nucleic acid encoding the two binding polypeptides and a peptide linker using techniques for nucleic acid synthesis, followed by expression of the nucleic acid thus obtained (as detailed further under the heading ‘preparative methods’ below).

Non-Protease-Labile Linkers

Suitably the non-protease-labile linker is a peptide and does not comprise a cleavage site for a protease.

Suitably the non-protease-labile linker is of the format -(G_(a)S_(b))_(x)— wherein a is 1 to 10, b is 1 to 5 and x is 1 to 15. More suitably a is 1 to 5, b is 1 to 2 and x is 1 to 10. More suitably a is 4, b is 1 and x is 1 to 8.

The TNF-alpha binding polypeptide and the IL-6R binding polypeptide, when linked to each other with a non-protease-labile linker, may be deployed in one of the following formats: anti-TNF-alpha-(G₄S)₆-anti-IL-6R (as exemplified by the particular construct ID-11K (residues 87-354 of SEQ ID NO: 21)), anti-IL-6R-(G₄S)₆-anti-TNF-alpha (as exemplified by the particular construct ID-12K (residues 87-354 of SEQ ID NO: 22)), anti-TNF-alpha-(G₄S)₂-anti-IL-6R (as exemplified by the particular construct ID-13K (residues 87-334 of SEQ ID NO: 23)), anti-TNF-alpha-(G₄S)₄-anti-IL-6R (as exemplified by the particular construct ID-14K (residues 87-344 of SEQ ID NO: 24)), anti-IL-6R-(G₄S)₂-anti-TNF-alpha or anti-IL-6R-(G₄S)₄-anti-TNF-alpha.

Most suitably the TNF-alpha binding polypeptide and the IL-6R binding polypeptide, when linked to each other with a non-protease-labile linker, are deployed in the format anti-TNF-alpha-(G₄S)₆-anti-IL-6R (as exemplified by the particular construct ID-11K (residues 87-354 of SEQ ID NO: 21)).

In one embodiment, the construct is selected from the list consisting of ID-11K (residues 87-354 of SEQ ID NO: 21), ID-12K (residues 87-354 of SEQ ID NO: 22), ID-13K (residues 87-334 of SEQ ID NO: 23) and ID-14K (residues 87-344 of SEQ ID NO: 24). More suitably, the construct is ID-11K.

Protease-Labile Linkers

A protease-labile linker (or ‘labile peptide linker’) is a peptide and comprises at least one cleavage site for a protease. Including a protease-labile linker in a construct of the invention allows, for example, the construct to be conveniently produced in the form of a heterobihead which is then later cleaved after administration into separate binding polypeptides.

In one embodiment of the invention, the labile peptide linker can be engineered such that it resists cleavage by proteases to a desired extent and/or is only cleaved upon exposure to a specific area of the intestinal tract. For example, if a construct is recombinantly produced in a host such as yeast, trypsin-like proteases produced by the yeast may cleave the recombinant construct product. This may result in difficulties in purification and cause regulatory, clinical and commercial complications.

This can be achieved by incorporating shielding residues into the labile peptide linker flanking the labile site(s). Shielding residues flank the labile site(s) of the labile peptide linker and reduce the lability thereof. Cleavage resistance can also be increased by positioning the labile site(s) closer to or at the periphery of the labile peptide linker. This concept is referred to as a “shielded labile site” and provides controlled lability.

The labile peptide linker can alternatively be engineered such that it is highly labile to cleavage by intestinal tract proteases, thereby quickly releasing the constituent polypeptides of the construct after oral administration. This is achieved by incorporating one or more labile sites into the labile peptide linker such that the labile site is exposed for proteolysis, for example by positioning the labile site(s) substantially centrally in the labile peptide linker and/or by the labile site not being shielded substantially by flanking residues. This concept is referred to as a “non-shielded labile site”.

Incorporation of a P residue into the labile peptide linker of the construct of the invention immediately following an R or K residue is expected to substantially prevent cleavage of the labile peptide linker. Suitably the labile peptide linker does not comprise any P residues.

Trypsin Labile Sites

Suitably the labile peptide linker comprises a cleavage site for trypsin or a trypsin-like protease. Suitably the labile peptide linker comprises at least 1, such as at least 2, such as at least 3, such as at least 4, such as at least 5, such as at least 6, such as at least 7, such as at least 8, such as at least 9, such as at least 10 K residues. Suitably the labile peptide linker comprises at least 1, such as at least 2, such as at least 3, such as at least 4, such as at least 5, such as at least 6, such as at least 7, such as at least 8, such as at least 9, such as at least 10 R residues. Preferably the cleavage site(s) is/are one or more K residue(s).

Non-Shielded Labile Sites

Suitably the protease-labile linker comprises or more suitably consists of the format [-(G_(a)S_(b))_(x)—B_(t)-(G_(c)S_(d))_(y)-]_(z) wherein B is lysine or arginine, t is 1 to 5, a is 0 to 10, b is 0 to 5, x is 0 to 10, c is 0 to 10, d is 0 to 5, y is 0 to 10 and z is 1 to 5. More suitably, B is lysine or arginine, t is 1 to 3, a is 0 to 5, b is 0 to 2, x is 0 to 5, c is 0 to 5, d is 0 to 2, y is 0 to 5 and z is 1 to 3. More suitably, t is 1, a is 3 to 5, b is 1, x is 1 to 2, c is 3 to 5, d is 1, y is 1 to 2 and z is 1.

Suitably the labile peptide linker comprises or more suitably consists of a polypeptide sequence of the format:

—B-(G_(a)S)_(x)—B′—

-   -   wherein     -   a is 1 to 10;     -   x is 1 to 10;     -   B is K or R and     -   B′ is K or R.

In one embodiment, a is 2 to 5, more suitably a is 4. In a further embodiment x is 1 to 5. More suitably, x is 2. B may be present or not present. B′ may be present or not present. Suitably, B is K. Suitably, B′ is K.

Particularly favoured linkers of this format are selected from one of the list consisting of —K-(G₄S)₂—K—, -(G₄S)₂—K—, —K-(G₄S)₂—, —R-(G₄S)₂—R—, -(G₄S)₂—R— and —R-(G₄S)₂—.

Suitably the labile peptide linker comprises or more suitably consists of a polypeptide sequence of the format:

—B-(G_(a)S)_(x)—B′-(G_(b)S)_(y)—B″—

-   -   wherein     -   a is 1 to 10;     -   b is 1 to 10;     -   x is 1 to 10;     -   y is 1 to 10;     -   B is K or R     -   B′ is K or R and     -   B″ is K or R.

In one embodiment, a is 2 to 5, more suitably a is 4. In one embodiment, b is 2 to 5, more suitably b is 4. In a further embodiment x is 1 to 5. More suitably, x is 2. In a further embodiment y is 1 to 5. More suitably, y is 2. Suitably, B is K. Suitably, B′ is K. Suitably, B″ is K.

Shielded Labile Sites

Shielding residues in the case of a trypsin or trypsin-like protease labile site may be D or E. Suitably the labile peptide linker comprises one or more shielding residues selected from the list consisting of D or E.

Suitably all K or R residues comprised within the labile peptide linker have at least 1, such as at least 2, such as at least 3, such as at least 4, such as at least 5 shielding residues on their N- and/or C-terminal side, wherein the shielding residues are selected from the list consisting of: D and E. Suitably all K or R residues comprised within the labile peptide linker have 1 to 5, 1 to 4, 1 to 3, 1 to 2, 2 to 5, 2 to 4, 2 to 3, 3 to 5, 3 to 4, 4 to 5 shielding residues on their N- and/or C-terminal side, wherein the shielding residues are selected from the list consisting of: D and E.

Suitably all K and R residues have at least one shielding residue adjacent to them, suitably followed by one or more further contiguous shielding residues. Suitably the shielding residues occur on one or both sides of one or more of the K or R residues.

Suitably the labile peptide linker comprises or more suitably consists of a polypeptide sequence of the format:

[-(G_(a)S)_(x)—U_(c)—B—U′_(d)-(G_(b)S)_(y)—]_(z)

-   -   wherein     -   a is 1 to 10;     -   b is 1 to 10;     -   U is D or E;     -   U′ is D or E;     -   c is 0 to 7;     -   d is 0 to 7;     -   x is 1 to 10;     -   y is 1 to 10     -   z is 1 to 10 and     -   B is K or R.

Suitably a is 2 to 5, more suitably a is 4. Suitably b is 2 to 5, more suitably b is 4. Suitably x is 1 to 5, more suitably x is 1. Suitably y is 1 to 5, more suitably y is 1. Suitably z is 1 to 3, more suitably z is 1. Suitably, B is K. Suitably, U if present, is D. Suitably, U′ if present, is D. In one embodiment c is 1 and d is 1. In another embodiment c is 0 and d is 0. In a further embodiment c is 4 and d is 0. Suitably both U and U′ are each individually D and c and d are both 1.

The TNF-alpha binding polypeptide and the IL-6R binding polypeptide, when linked to each other with a protease labile linker, may be deployed in one of the following specific formats:

Anti-TNF-alpha-G₄S—K-G₄S-anti-IL-6R, anti-IL-6R-G₄S—K-G₄S-anti-TNF-alpha, anti-TNF-alpha-G₄S-KD-G₄S-anti-IL-6R anti-IL-6R-G₄S-KD-G₄S-anti-TNF-alpha, anti-TNF-alpha-G₄S-DK-G₄S-anti-IL-6R, anti-IL-6R-G₄S-DK-G₄S-anti-TNF-alpha, anti-TNF-alpha-G₄S-DKD-G₄S-anti-IL-6R, anti-IL-6R-G₄S-DKD-G₄S-anti-TNF-alpha, anti-TNF-alpha-G₄S—R-G₄S-anti-IL-6R, anti-IL-6R-G₄S—R-G₄S-anti-TNF-alpha, anti-TNF-alpha-G₄S-RD-G₄S-anti-IL-6R, anti-IL-6R-G₄S-RD-G₄S-anti-TNF-alpha, anti-TNF-alpha-G₄S-DR-G₄S-anti-IL-6R, anti-IL-6R-G₄S-DR-G₄S-anti-TNF-alpha, anti-TNF-alpha-G₄S-DRD-G₄S-anti-IL-6R or anti-IL-6R-G₄S-DRD-G₄S-anti-TNF-alpha.

In further embodiments, the TNF-alpha binding polypeptide and the IL-6R binding polypeptide, when linked to each other, may be deployed in one of the above formats except that any one or more (for example, all) of the D residues above are substituted with one or more E residues.

More suitably, the TNF-alpha binding polypeptide and the IL-6R binding polypeptide, when linked to each other with a protease labile linker, may be deployed in either anti-TNF-alpha-G₄S—K-G₄S-anti-IL-6R format (as exemplified by specific construct ID-9K (residues 87-335 of SEQ ID NO: 19)) or anti-IL-6R-G₄S—K-G₄S-anti-TNF-alpha format (as exemplified by specific construct ID-10K (residues 87-335 of SEQ ID NO: 20)). Most suitably, they may be deployed in anti-TNF-alpha-G₄S—K-G₄S-anti-IL-6R format.

In one embodiment, the construct is selected from the list consisting of ID-9K (residues 87-335 of SEQ ID NO: 19) and ID-10K (residues 87-335 of SEQ ID NO: 20). More suitably, the construct is ID-9K.

Chymotrypsin Labile Sites

Alternatively, or in addition to trypsin labile sites, the labile peptide linker of the construct may comprise a cleavage site for chymotrypsin or a chymotrypsin-like protease. Suitably the labile peptide linker comprises at least 1, such as at least 2, such as at least 3, such as at least 4, such as at least 5, such as at least 6, such as at least 7, such as at least 8, such as at least 9, such as at least 10 residues selected from the list consisting of W, F, Y, L and M; more suitably W, F and Y. Suitably the labile peptide linker consists of residues selected from the list consisting of S, G, W, F, Y, L and M; such as S, G, W, F and Y.

Suitably the protease-labile linker is of the format [-(G_(a)S_(b))_(x)-J_(t)-(G_(c)S_(d))_(y)-]_(z) wherein J is W, F, Y, L or M, t is 0 to 5, a is 0 to 10, b is 0 to 5, x is 0 to 10, c is 0 to 10, d is 0 to 5, y is 0 to 10 and z is 1 to 5. More suitably, J is W, F, Y, L or M, t is 0 to 3, a is 0 to 5, b is 0 to 2, x is 0 to 5, c is 0 to 5, d is 0 to 2, y is 0 to 5 and z is 1 to 3.

Suitably the labile peptide linker comprises or more suitably consists of a polypeptide sequence of the format:

[-(G_(a)S)_(x)-J-(G_(b)S)_(y)-]_(z)

-   -   wherein         -   a is 1 to 10;         -   b is 1 to 10;         -   x is 1 to 10;         -   y is 1 to 10         -   z is 1 to 10 and         -   J is W, F, Y, L or M; such as W, F or Y.

In one embodiment a is 2 to 5, in a further embodiment, b is 2 to 5, in a further embodiment x is 1 to 5, in a further embodiment, y is 1 to 5, in a further embodiment z is 1 to 3. Suitably x is 1, y is 1 and z is 1.

Suitably the labile peptide linker comprises or more suitably consists of a polypeptide sequence of the format:

[-(G₄S)_(x)-J-(G₄S)_(y)—]_(z)

-   -   wherein         -   x is 1 to 10;         -   y is 1 to 10         -   z is 1 to 10 and         -   J is W, F, Y, L or M; such as W, F or Y.

In one embodiment, x is 1 to 5, in a further embodiment, y is 1 to 5, in a further embodiment z is 1 to 3. Suitably x is 1, y is 1 and z is 1.

Enterokinase Labile Sites

Alternatively, or in addition to trypsin and/or chymotrypsin labile sites, the labile peptide linker of the construct may comprise a cleavage site for an enterokinase. Suitably the labile peptide linker comprises the sequence DDDDK (SEQ ID NO: 31), such as a sequence comprising or consisting of -G₄S-DDDDK-G₄S—.

MMP Labile Sites

In one embodiment, the labile peptide linker of the construct may comprise a cleavage site for MMP3, MMP10 or MMP12.

Other Labile Sites

In one embodiment, the labile peptide linker of the construct may comprise a cleavage site for other inflammatory or microbial proteases wherein the cleavage site is known.

Stability of Labile Peptide Linkers to Expression Hosts

Various organisms may be used to express recombinant polypeptides. Commonly used expression organisms include yeast, mould and mammalian cells. However, many of these expression organisms also produce proteases, such as trypsin-like proteases, which may cleave the expressed recombinant polypeptide. If the expressed polypeptide incorporates a peptide linker which is labile to one or more proteases present in the intestinal tract, then this peptide linker may undesirably also be labile to proteases produced by the expression organism, thus preventing effective expression of intact polypeptide.

It is advantageous for the labile peptide linker to be substantially non-labile to enzymes produced by the recombinant host used to produce the construct. Suitably the labile peptide linker is substantially resistant to proteases produced by a recombinant host such as bacteria such as E. coli or such as a yeast or mould belonging to the genera Aspergillus, Saccharomyces, Kluyveromyces, Hansenula or Pichia; such as Saccharomyces cerevisiae or Pichia pastoris.

Suitably the recombinant host is a yeast or a mould. Suitably the yeast belongs to the genera Saccharomyces, Kluyveromyces, Hansenula, Pichia, Candida or Torulopsis. Suitably the mould belongs to the genus Aspergillus, Acremonium, Alternaria, Chrysosporium, Cladosporium, Dictyostelium, Fusarium, Mucor, Penicillium, Rhizopus, Stachybotrys, Trichoderma and Trichophyton.

The Gastrointestinal Tract and Digestive Enzymes

The gastrointestinal tract (GIT) is an organ system responsible for consuming and digesting foodstuffs, absorbing nutrients, and expelling waste. In humans and other mammals, the GIT consists of the oesophagus, stomach, small intestine (duodenum, jejunum and ileum) and large intestine (cecum, colon, rectum and anal canal). Various pathogens may colonise and various diseases may manifest in different areas of the GIT. The intestinal tract (as opposed to the gastrointestinal tract) consists of the small and large intestine.

The different parts of the gastrointestinal tract each contain a complex mixture of digestive enzymes. Proteases are involved in digesting polypeptide chains into shorter fragments by splitting the peptide bonds that link amino acid residues (proteolysis). Some detach the terminal amino acids from the protein chain (exopeptidases), others attack internal peptide bonds of a protein (endopeptidases). Proteolysis can be highly promiscuous such that a wide range of protein substrates are hydrolysed. This is the case for proteases which cleave the wide array of ingested polypeptides in the intestinal tract into smaller polypeptide fragments.

Many proteases typically bind to a single amino acid (a labile site) on the substrate and so only have specificity for that residue. The proteases present in the intestinal tract include trypsin, trypsin-like proteases, chymotrypsin, chymotrypsin-like proteases, carboxypeptidase, elastase, aminopeptidase, carboxypeptidase and enteropeptidase. Trypsin-like proteases cleave peptide bonds following lysine or arginine residues. Chymotrypsin-like proteases cleave peptide bonds following hydrophobic residues, such as tyrosine, phenylalanine, tryptophan, leucine and methionine. Particularly tyrosine, phenylalanine and tryptophan.

Particularly in the context of an oral medicament, it may be desirable for the binding polypeptides to be substantially resistant to one or more (such as all) proteases of the intestinal tract, while the labile peptide linker (if used) is labile to one or more (such as all) proteases of the intestinal tract.

Suitably the polypeptides in the construct are substantially resistant to one or more proteases and suitably the labile peptide linker (if present) is labile to one or more proteases, wherein said one or more proteases are present in the small or large intestine, more suitably the jejunum, the ileum and/or the cecum. A substantially resistant polypeptide substantially retains neutralisation ability and/or potency when exposed to one or more proteases.

Such proteases include proteases sourced from gastrointestinal tract commensal microflora or pathogenic bacteria, for example wherein the proteases are cell membrane-attached proteases, secreted proteases and proteases released on cell lysis. Such proteases may also include IBD inflammatory proteases such as MMP3, MMP10 and MMP12. Suitably the one or more proteases are serine proteases. Suitably the one or more proteases are selected from the group consisting of enteropeptidase, trypsin, trypsin-like proteases, chymotrypsin and chymotrypsin-like proteases.

Suitably, the polypeptides substantially retain neutralisation ability and/or potency when delivered orally and after exposure to the intestinal tract (for example, after exposure to proteases of the small and/or large intestine and/or IBD inflammatory proteases). Proteases of, or produced in, the small and/or large intestine include proteases sourced from intestinal commensal microflora and/or pathogenic bacteria, for example wherein the proteases are cell membrane-attached proteases, excreted proteases and proteases released on cell lysis). Most suitably the proteases are trypsin and chymotrypsin.

Suitably the intestinal tract is the intestinal tract of a dog, pig, rat, guinea pig, hamster, rabbit, human, cynomolgus monkey or mouse. The small intestine suitably consists of the duodenum, jejunum and ileum. The large intestine suitably consists of the cecum, colon, rectum and anal canal.

The polypeptides substantially retain neutralisation ability when suitably at least 10%, more suitably 20%, more suitably 30%, more suitably 40%, more suitably 50%, more suitably 60%, more suitably 70%, more suitably 80%, more suitably 90%, more suitably 95%, more suitably 100% of the original neutralisation ability of the polypeptides or construct is retained after exposure to proteases present in the small and/or large intestine and/or IBD inflammatory proteases; after a given time period of exposure at a given temperature. This concept is referred to herein as ‘% survival’.

Suitably the polypeptide substantially retains neutralisation ability after exposure to proteases present in the small and/or large intestine and/or IBD inflammatory proteases for, for example, up to at least 2, more suitably up to at least 3, more suitably up to at least 4, more suitably up to at least 5, more suitably up to at least 5.5, more suitably up to at least 16, more suitably up to at least 21 or more suitably up to at least 22 hours, at 37 degrees C.

Suitably 10% or more, more suitably 20% or more, more suitably 30% or more, more suitably 40% or more, more suitably 50% or more, more suitably 60% or more, more suitably 70% or more of the neutralisation ability of the polypeptides is retained after 4, 6, 7 or 16 hours of exposure to conditions of the intestinal tract, more suitably the small or large intestine, more suitably human faecal extract.

Suitably 10% or more, more suitably 20% or more, more suitably 30% or more, more suitably 40% or more, more suitably 50% or more, more suitably 60% or more, more suitably 70% or more of the neutralisation ability of the polypeptides is retained after suitably 4, 6, 7 or 16 hours of exposure to mouse small intestinal supernatant.

Autoimmune Diseases and/or Inflammatory Diseases

The compositions and constructs provided by the invention may in particular find utility in the prevention or treatment of autoimmune diseases and/or inflammatory diseases.

Autoimmune diseases develop when the immune system responds adversely to normal body tissues. Autoimmune disorders may result in damage to body tissues, abnormal organ growth and/or changes in organ function. The disorder may affect only one organ or tissue type or may affect multiple organs and tissues. Organs and tissues commonly affected by autoimmune disorders include blood components such as red blood cells, blood vessels, connective tissues, endocrine glands such as the thyroid or pancreas, muscles, joints and skin. An inflammatory disease is a disease characterised by inflammation. Many inflammatory diseases are autoimmune diseases and vice-versa.

Autoimmune Diseases and/or Inflammatory Diseases of the GIT

The chronic inflammatory bowel diseases (IBD) Crohn's disease and ulcerative colitis, which afflict both children and adults, are examples of autoimmune and inflammatory diseases of the GIT (Hendrickson et al 2002, herein incorporated by reference in its entirety). Ulcerative colitis is defined as a condition where the inflammatory response and morphologic changes remain confined to the colon. The rectum is involved in 95% of patients. Inflammation is largely limited to the mucosa and consists of continuous involvement of variable severity with ulceration, edema, and hemorrhage along the length of the colon (Hendrickson et al 2002, herein incorporated by reference in its entirety). Ulcerative colitis is usually manifested by the presence of blood and mucus mixed with stool, along with lower abdominal cramping which is most severe during the passage of bowel movements. Clinically, the presence of diarrhoea with blood and mucus differentiates ulcerative colitis from irritable bowel syndrome, in which blood is absent. Unlike ulcerative colitis, the presentation of Crohn's disease is usually subtle, which leads to a later diagnosis. Factors such as the location, extent, and severity of involvement determine the extent of gastrointestinal symptoms. Patients who have ileocolonic involvement usually have postprandial abdominal pain, with tenderness in the right lower quadrant and an occasional inflammatory mass. Symptoms associated with gastroduodenal Crohn's disease include early satiety, nausea, emesis, epigastric pain, or dysphagia. Perianal disease is common, along with anal tags, deep anal fissures, and fistulae (Hendrickson et al 2002, herein incorporated by reference in its entirety).

In these diseases the TNF-alpha is produced in the lamina propria underlying the gastrointestinal epithelium. This epithelium is disrupted in IBD and facilitates transport of the immunoglobulin chain variable domain into the lamina propria—the site of TNF-alpha production and biological action in these diseases. Other diseases of the GIT include for example the inflammatory disease mucositis (suitably drug- and radiation induced-mucositis) where inflammatory lesions are present in the mucosa disrupting the epithelial tight junctions which also allow the compositions of the invention access to the site of TNF-alpha production.

In mucositis the lesions can occur anywhere from mouth to anus and for mouth and oesophagus lesions a mouthwash or cream preparation containing the composition may be used. For anal and rectal lesions, suppositories, creams or foams containing the composition would be suitable for topical application. The composition will be cleared from the lamina propria or other inflammatory sites via absorption into the bloodstream at sites of inflammation or via lympatic clearance and subsequent entry into the bloodstream. The composition will therefore reach the liver via the bloodstream and will be cleared via glomerular filtration in the kidney. There is therefore good rationale that the composition of the invention will function therapeutically in diseases such as autoimmune hepatitis, type II diabetes and glomerular nephritis.

Interleukin-6 is a proinflammatory cytokine that is considered to be involved in the pathogenesis of IBD and IL6-trans-signalling via soluble IL6-R is thought to play a particularly important role in mediating effects of IL-6 associated with the perpetuation of chronic intestinal inflammation (see Mitsuyama et al., 2007). High levels of IL-6 production have been found in cultured CD and UC intestinal mucosal biopsies (Gustot et al., 2005; Kusugami et al., 1995; Reimund et al., 1996; Hosokawa et al., 1999) associated with increased levels of slL-6R production (Hosokawa, 1999). Levels of IL-6 and slL-6R production were greater in “involved” vs “non-involved” IBD tissue and were correlated with the severity of clinical disease. Lamina propria cells were found to be major producers of IL-6 (Reinecker et al., 1993; Kusugami et al., 1995; Reimund et al., 1996; Hosokawa et al., 1999) and slL6Rs (Hosokawa et al., 1999). In cell cultures, IBD mucosal tissue-derived macrophages were the main cell type producing IL-6 (Kusugami et al., 1995) and slL6R (Hosokawa et al., 1999) on a per cell basis, while T cells, B cells and epithelial cells produced substantially lower amounts. Interestingly, the levels of IL-6 production by IBD tissue and tissue derived cells far exceeded the levels of slL6R production (see Hosokawa et al., 1999).

In inflamed IBD tissue, the production of IL-6 and shedding of IL-6Rs from activated macrophages results in the formation of soluble IL-6/slL-6R complexes that can activate trans-signalling in cells that express only the gp130 subunit. This mechanism, which extends IL-6 responsiveness to an increased number of target cells, is considered to play an important role in the orchestration of mucosal inflammatory processes. The mechanism of IL-6 induced intestinal epithelial cell proliferation and regeneration is thought to involve signal transduction mediated via membrane bound IL-6 receptors (cis-signalling) (Rose-John, 2012; Waetzig & Rose-John 2012). The anti-human IL-6R antibody tocilizumab blocks both IL-6R classical signalling and IL-6/slL-6R mediated trans-signalling and therefore blocks both pro-inflammatory, and potentially protective activities of IL-6. A rationale for the development of selective antagonists of IL-6-trans-signalling has been proposed based on the concept that this might avoid the inhibition of beneficial epithelial regenerative effects of IL-6 (see Rose-John et al, 2012; Waetzig & Rose-John 2012) that are mediated via mIL-6Rs (cis-signalling). An oral pharmaceutical product with this profile could have safety and efficacy advantages over existing IL-6 neutralising antibodies for the treatment of Crohn's disease based on anti-inflammatory and improved mucosal healing properties.

Suitably the composition of the invention is used in the treatment or prevention of an autoimmune and/or inflammatory disease of the GI (gastrointestinal) tract.

Suitably the composition of the invention is for use in the treatment of an autoimmune and/or inflammatory disease of the GI tract selected from the list consisting of Crohn's disease, ulcerative colitis, irritable bowel disease, diabetes type II, glomerulonephritis, autoimmune hepatitis, Sjogren's syndrome, celiac disease and drug- or radiation-induced mucositis (more suitably Crohn's disease or ulcerative colitis, most suitably Crohn's disease).

Oral delivery of the composition will ideally treat inflammatory diseases where TNF-alpha and/or IL-6R (or IL-6) contributes to at least a proportion of the pathology and more suitably wherein the immunoglobulin chain variable domain can access the tissue where the TNF-alpha and/or IL-6R is biologically active.

Autoimmune Diseases and/or Inflammatory Diseases of the Skin

Psoriasis is a debilitating autoimmune, dermatological, disease. Plaque psoriasis, the most common form of the disease, is characterized by red skin covered with silvery scales. Histologically the picture is one of disordered differentiation and hyperproliferation of keratinocytes within the psoriatic plaque with inflammatory cell infiltrates (Ortonne, 1999). The psoriatic skin lesions are inflammatory, red, sharply delimited plaques of various shapes with characteristic silvery lustrous scaling. The term psoriasis includes psoriasis and the symptoms of psoriasis including erythema, skin thickening/elevation and scaling.

Biological agents of use in the treatment of psoriasis include anti-TNF-alpha therapies (such as monoclonal antibodies against TNF, e.g. adalimumab and infliximab, or TNF-alpha receptor fusion proteins such as etanercept), humanised antibodies to CDIIa (efalizumab) or agents which bind to CD2 such as alefacept (thereby blocking the CD2 LFA3 interaction). It should be noted that not all of the biological agents listed here have been approved for use in the treatment of psoriasis.

The composition of the invention may be incorporated into a cream/ointment or other topical carrier for administration to inflammatory skin lesions where TNF-alpha and/or IL-6R or IL-6 contributes to the pathology of such lesions.

Suitably the composition of the invention is for use in the treatment of an autoimmune and/or inflammatory disease of the skin selected from the list consisting of pemphigus, psoriasis, eczema and scleroderma.

Therapeutic Use and Delivery

Suitably the composition of the invention is for use as a medicament, suitably administered by oral administration, suitably for use in the treatment or prevention of diseases of the GIT and/or the treatment or prevention of diseases such as autoimmune disease and/or inflammatory disease, such as inflammatory bowel disease. The composition of the invention may also be used in the treatment or prevention of other medical conditions by oral administration such as metabolic disorders, such as obesity. In one embodiment, the composition of the invention is intended to have local effect in the intestinal tract. In one embodiment, the composition of the invention is not for use in the treatment or prevention of diseases by delivery into the circulation in therapeutically effective quantities.

In one aspect of the invention there is provided a method of treating autoimmune disease and/or inflammatory disease comprising administering to a person in need thereof a therapeutically effective amount of the inventive composition.

The anti-TNF-alpha binding polypeptide and the anti-IL-6R binding polypeptide may be co-formulated in a composition of the invention or alternatively may be separately formulated and administered separately, sequentially or simultaneously.

The TNF-alpha binding polypeptide and the IL-6R binding polypeptide may be administered by the same route or by different routes. For example, the TNF-alpha binding polypeptide may be administered orally while the IL-6R binding polypeptide may be administered rectally.

In one aspect of the invention, there is provided a TNF-alpha binding polypeptide for use in the treatment or prevention of an autoimmune disease and/or inflammatory disease, together with an IL-6R binding polypeptide. In a further aspect, there is provided an IL-6R binding polypeptide for use in the treatment or prevention of an autoimmune disease and/or inflammatory disease, together with a TNF-alpha binding polypeptide.

In a further aspect of the invention there is provided a method of treating autoimmune disease and/or inflammatory disease comprising administering to a person in need thereof a TNF-alpha binding polypeptide, together with an IL-6R binding polypeptide. There is also provided a method of treating autoimmune disease and/or inflammatory disease comprising administering to a person in need thereof an IL-6R binding polypeptide, together with a TNF-alpha binding polypeptide.

In a further aspect of the invention there is provided a composition comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide for use in the treatment or prevention of inflammatory bowel disease and/or mucositis.

In a further aspect of the invention there is provided a composition comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide for use in the treatment or prevention of inflammatory bowel disease and/or mucositis, wherein the composition is orally administered.

In a further aspect of the invention there is provided the use of a composition comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide in the manufacture of a medicament for the treatment or prevention of inflammatory bowel disease and/or mucositis.

In a further aspect of the invention there is provided the use of a composition comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide in the manufacture of a medicament for the treatment or prevention of inflammatory bowel disease and/or mucositis by oral administration.

In a further aspect of the invention there is provided a method of treating or preventing inflammatory bowel disease and/or mucositis comprising administering to a person in need thereof a composition comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide.

In a further aspect of the invention there is provided a method of treating or preventing inflammatory bowel disease and/or mucositis comprising orally administering to a person in need thereof a composition comprising a TNF-alpha binding polypeptide and an IL-6R binding polypeptide.

In the embodiments above, the inflammatory bowel disease is suitably Crohn's disease or ulcerative colitis, most suitably Crohn's disease. Furthermore, in the embodiments above, the TNF-alpha binding polypeptide is suitably a polypeptide comprising an antibody fragment and/or the IL-6R binding polypeptide is suitably a polypeptide comprising an antibody fragment. Most suitably, the TNF-alpha binding polypeptide and the IL-6R binding polypeptide are both polypeptides comprising an antibody fragment.

Administration of one binding polypeptide ‘together’ with another binding polypeptide means that the therapeutic windows of each binding polypeptide overlap with each other. This means that, for example, a therapeutically effective amount of each binding polypeptide is present in the body of the subject at the same time. In a particular embodiment, a therapeutically effective amount of each binding polypeptide is present at the site of therapeutic need at the same time.

A therapeutically effective amount of a composition of the invention is an amount which is effective, upon single or multiple dose administration to a subject, in neutralising the biological effects of a chosen target to a significant extent in a subject. A therapeutically effective amount may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of the construct to elicit a desired response in the individual. A therapeutically effective amount is also one in which any toxic or detrimental effects of the construct are outweighed by the therapeutically beneficial effects. The composition of the invention can be incorporated into pharmaceutical compositions suitable for oral administration to a subject.

A composition of the invention may be formulated for oral delivery. The compositions of the invention may be in a variety of forms. These include, for example, liquid, semi-solid and solid dosage forms, such as liquid solutions, dispersions or suspensions, tablets, pills and powders. Solid dosage forms are preferred. The composition may comprise a pharmaceutically acceptable excipient, and suitably may be used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like.

Typically, the composition comprises a pharmaceutically acceptable excipient such as a carrier, forming a pharmaceutical composition. Examples of pharmaceutically acceptable carriers include one or more of water, saline, phosphate buffered saline, dextrose, glycerol, ethanol and the like, as well as combinations thereof. Pharmaceutically acceptable carriers may further comprise minor amounts of auxiliary substances such as wetting or emulsifying agents, preservatives or buffers, which enhance the shelf life or effectiveness of the polypeptide or construct of the invention. Pharmaceutical compositions may include antiadherents, binders, coatings, disintegrants, flavours, colours, lubricants, sorbents, preservatives, sweeteners, freeze dry excipients (including lyoprotectants) or compression aids. Suitably, the polypeptides in the composition of the invention are lyophilised before being incorporated into a pharmaceutical composition.

A composition of the invention may also be provided with an enteric coating. An enteric coating is a polymer barrier applied on oral medication which protects the polypeptide from the low pH of the stomach. Materials used for enteric coatings include fatty acids, waxes, shellac, plastics, and plant fibers. Suitable enteric coating components include methyl acrylate-methacrylic acid copolymers, cellulose acetate succinate, hydroxy propyl methyl cellulose phthalate, hydroxy propyl methyl cellulose acetate succinate (hypromellose acetate succinate), polyvinyl acetate phthalate (PVAP), methyl methacrylate-methacrylic acid copolymers, sodium alginate and stearic acid. Suitable enteric coatings include pH-dependent release polymers. These are polymers which are insoluble at the highly acidic pH found in the stomach, but which dissolve rapidly at a less acidic pH. Thus, suitably, the enteric coating will not dissolve in the acidic juices of the stomach (pH ˜3), but will do so in the higher pH environment present in the small intestine (pH above 6) or in the colon (pH above 7.0). The pH-dependent release polymer is selected such that the composition of the invention will be released at about the time that the dosage reaches the target region of the intestinal tract.

The pharmaceutical composition of the invention may be formulated in a buffer, in order to stabilise the pH of the composition, at a concentration between 5-50, or more suitably 15-40 or more suitably 25-30 g/litre. Examples of suitable buffer components include physiological salts such as sodium citrate and/or citric acid. Suitably buffers contain 100-200, more suitably 125-175 mM physiological salts such as sodium chloride. Suitably the buffer is selected to have a pKa close to the pH of the composition or the physiological pH of the patient.

Exemplary concentrations of polypeptide in a pharmaceutical composition may range from about 1 mg/mL to about 200 mg/ml or from about 50 mg/mL to about 200 mg/mL, or from about 150 mg/mL to about 200 mg/mL.

An aqueous formulation of the pharmaceutical composition of the invention may be prepared in a pH-buffered solution, e.g., at pH ranging from about 4.0 to about 7.0, or from about 5.0 to about 6.0, or alternatively about 5.5. Examples of suitable buffers include phosphate-, histidine-, citrate-, succinate-, acetate-buffers and other organic acid buffers. The buffer concentration can be from about 1 mM to about 100 mM, or from about 5 mM to about 50 mM, depending, for example, on the buffer and the desired tonicity of the formulation.

The tonicity of the pharmaceutical composition may be altered by including a tonicity modifier. Such tonicity modifiers can be charged or uncharged chemical species. Typical uncharged tonicity modifiers include sugars or sugar alcohols or other polyols, preferably trehalose, sucrose, mannitol, glycerol, 1,2-propanediol, raffinose, sorbitol or lactitol (especially trehalose, mannitol, glycerol or 1,2-propanediol). Typical charged tonicity modifiers include salts such as a combination of sodium, potassium or calcium ions, with chloride, sulfate, carbonate, sulfite, nitrate, lactate, succinate, acetate or maleate ions (especially sodium chloride or sodium sulphate); or amino acids such as arginine or histidine. Suitably, the aqueous formulation is isotonic, although hypertonic or hypotonic solutions may be suitable. The term “isotonic” denotes a solution having the same tonicity as some other solution with which it is compared, such as physiological salt solution or serum. Tonicity agents may be used in an amount of about 5 mM to about 350 mM, e.g., in an amount of 1 mM to 500 nM. Suitably, at least one isotonic agent is included in the composition.

A surfactant may also be added to the pharmaceutical composition to reduce aggregation of the formulated construct and/or minimize the formation of particulates in the formulation and/or reduce adsorption. Exemplary surfactants include polyoxyethylensorbitan fatty acid esters (Tween), polyoxyethylene alkyl ethers (Brij), alkylphenylpolyoxyethylene ethers (Triton-X), polyoxyethylene-polyoxypropylene copolymer (Poloxamer, Pluronic), and sodium dodecyl sulfate (SDS). Examples of suitable polyoxyethylenesorbitan-fatty acid esters are polysorbate 20, and polysorbate 80. Exemplary concentrations of surfactant may range from about 0.001% to about 10% w/v.

A lyoprotectant may also be added in order to protect the polypeptides against destabilizing conditions during the lyophilization process. For example, known lyoprotectants include sugars (including glucose, sucrose, mannose and trehalose); polyols (including mannitol, sorbitol and glycerol); and amino acids (including alanine, glycine and glutamic acid). Lyoprotectants can be included in an amount of about 10 mM to 500 mM.

The dosage ranges for administration of the pharmaceutical composition of the invention are those to produce the desired therapeutic effect. The dosage range required depends on the precise nature of the pharmaceutical composition or construct, the target region of the intestinal tract, the nature of the formulation, the age of the patient, the nature, extent or severity of the patient's condition, contraindications, if any, and the judgement of the attending physician. Variations in these dosage levels can be adjusted using standard empirical routines for optimisation.

Suitable daily dosages of pharmaceutical composition of the invention are in the range of 50 ng-50 mg per kg, such as 50 ug-40 mg per kg, such as 5-30 mg per kg of body weight. The unit dosage can vary from less than 100 mg, but typically will be in the region of 250-2000 mg per dose, which may be administered daily or more frequently, for example 2, 3 or 4 times per day or less frequently for example every other day or once per week.

The TNF-alpha binding polypeptide and the IL-6R binding polypeptide, when present in the inventive composition and when not linked to each other, may be present in a TNF-alpha binding polypeptide to IL-6R binding polypeptide molar ratio of 20:1 to 1:20, such as 15:1 to 1:15, more suitably 10:1 to 1:10, more suitably 5:1 to 1:5, more suitably 3:1 to 1:3, more suitably 2:1 to 1:2, more suitably 1.5:1 to 1:1.5, most suitably about 1:1.

Treatment of diseases also embraces treatment of exacerbations thereof, amelioration of symptoms thereof and also embraces treatment of patients in remission from disease symptoms to prevent relapse of disease symptoms.

Combination Therapy

A pharmaceutical composition of the invention may also comprise one or more active agents (e.g. active agents suitable for treating diseases such as those mentioned herein). It is within the scope of the invention to use the pharmaceutical composition of the invention in therapeutic methods for the treatment of autoimmune and/or inflammatory diseases as an adjunct to, or in conjunction with, other established therapies normally used in the treatment of bacterial, autoimmune and/or inflammatory diseases.

For the treatment of irritable bowel disease (such as Crohn's disease or ulcerative colitis), possible combinations include combinations with, for example, one or more active agents selected from the list comprising: 5-aminosalicylic acid, or a prodrug thereof (such as sulfasalazine, olsalazine or bisalazide); corticosteroids (e.g. prednisolone, methylprednisolone, or budesonide); immunosuppressants (e.g. cyclosporin, tacrolimus, methotrexate, azathioprine or 6-mercaptopurine); anti-TNF-alpha antibodies (e.g., infliximab, adalimumab, certolizumab pegol or golimumab); anti-lL12/IL23 antibodies (e.g., ustekinumab); anti-IL6R antibodies or small molecule IL12/IL23 inhibitors (e.g., apilimod); Anti-alpha-4-beta-7 antibodies (e.g., vedolizumab); MAdCAM-1 blockers (e.g., PF-00547659); antibodies against the cell adhesion molecule alpha-4-integrin (e.g., natalizumab); antibodies against the IL2 receptor alpha subunit (e.g., daclizumab or basiliximab); JAK3 inhibitors (e.g., tofacitinib or R348); Syk inhibitors and prodrugs thereof (e.g., fostamatinib and R-406); Phosphodiesterase-4 inhibitors (e.g., tetomilast); HMPL-004; probiotics; Dersalazine; semapimod/CPSI-2364; and protein kinase C inhibitors (e.g. AEB-071). The most suitable combination agents are infliximab, adalimumab, certolizumab pegol or golimumab.

Hence another aspect of the invention provides a pharmaceutical composition of the invention in combination with one or more further active agents, for example one or more active agents described above. In a further aspect of the invention, the pharmaceutical composition or construct is administered sequentially, simultaneously or separately with at least one active agent selected from the list above.

Similarly, another aspect of the invention provides a combination product comprising:

(A) a pharmaceutical composition of the present invention; and

(B) one or more other active agents,

wherein each of components (A) and (B) is formulated in admixture with a pharmaceutically-acceptable adjuvant, diluent or carrier. In this aspect of the invention, the combination product may be either a single (combination) formulation or a kit-of-parts. Thus, this aspect of the invention encompasses a combination formulation including a pharmaceutical composition or construct of the present invention and another therapeutic agent, in admixture with a pharmaceutically acceptable adjuvant, diluent or carrier.

The invention also encompasses a kit of parts comprising components:

(i) a pharmaceutical composition of the present invention in admixture with a pharmaceutically acceptable adjuvant, diluent or carrier; and

(ii) a formulation including one or more other active agents, in admixture with a pharmaceutically-acceptable adjuvant, diluent or carrier, which components (i) and (ii) are each provided in a form that is suitable for administration in conjunction with the other.

Component (i) of the kit of parts is thus component (A) above in admixture with a pharmaceutically acceptable adjuvant, diluent or carrier. Similarly, component (ii) is component (B) above in admixture with a pharmaceutically acceptable adjuvant, diluent or carrier. The one or more other active agents (i.e. component (B) above) may be, for example, any of the agents mentioned above in connection with the treatment of bacterial infection such as Clostridium difficile infection, autoimmune and/or inflammatory diseases such as IBD (e.g. Crohn's disease and/or ulcerative colitis). If component (B) is more than one further active agent, these further active agents can be formulated with each other or formulated with component (A) or they may be formulated separately. In one embodiment component (B) is one other therapeutic agent. In another embodiment component (B) is two other therapeutic agents. The combination product (either a combined preparation or kit-of-parts) of this aspect of the invention may be used in the treatment or prevention of an autoimmune disease (e.g. the autoimmune diseases mentioned herein).

Vectors and Hosts

The term “vector”, as used herein, is intended to refer to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. One type of vector is a plasmid, which refers to a circular double stranded DNA loop into which additional DNA segments may be ligated. Another type of vector is a viral vector, wherein additional DNA segments may be ligated into the viral genome. Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors having a bacterial origin of replication and episomal mammalian and yeast vectors). Other vectors (e.g. non-episomal mammalian vectors) can be integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome. Moreover, certain vectors are capable of directing the expression of genes to which they are operatively linked. Such vectors are referred to herein as “recombinant expression vectors” (or simply, “expression vectors”). In general, expression vectors of utility in recombinant DNA techniques are often in the form of plasmids. In the present specification, “plasmid” and vector” may be used interchangeably as the plasmid is the most commonly used form of vector. However, the invention is intended to include such other forms of expression vectors, such as viral vectors (e.g. replication defective retroviruses, adenoviruses and adeno-associated viruses), which serve equivalent functions, and also bacteriophage and phagemid systems. The invention also relates to nucleotide sequences that encode the polypeptides in the composition of the invention. The term “recombinant host cell” (or simply “host cell”), as used herein, is intended to refer to a cell into which a recombinant expression vector has been introduced. Such terms are intended to refer not only to the particular subject cell but to the progeny of such a cell.

In one aspect of the invention there is provided a vector comprising the polynucleotide encoding a construct of the invention or cDNA comprising said polynucleotide. In a further aspect of the invention there is provided a host cell transformed with said vector, which is capable of expressing the construct of the invention. Suitably the host cell is a yeast such as a yeast belonging to the genera Aspergillus, Saccharomyces, Kluyveromyces, Hansenula or Pichia, such as Saccharomyces cerevisiae, Escherchia coli or Pichia pastoris.

The specific constructs ID-9K to ID-14K disclosed herein as SEQ ID NO: 19 to SEQ ID NO: 24 each comprise an export signal sequence which is the yeast mating factor alpha secretion sequence (MFal). Other suitable export signal sequences include the yeast invertase (SUC2) signal, the acid phosphatase (PHOS) signal sequence (Romanos et al 1992) and the BGL2 gene signal sequence (Achstetter et al 1992). These and other export signal sequences can equally be used in combination with unlinked anti-TNF-alpha binding polypeptides and anti-IL-6R binding polypeptides such as ID-38F and ID-142V disclosed herein.

Preparative Methods

Polypeptides and constructs comprising polypeptides can be obtained and manipulated using the techniques disclosed for example in Green and Sambrook 2012.

Monoclonal antibodies can be produced using hybridoma technology, by fusing a specific antibody-producing B cell with a myeloma (B cell cancer) cell that is selected for its ability to grow in tissue culture and for an absence of antibody chain synthesis (Köhler et al., 1975 and Nelson et al., 2000, herein incorporated by reference in their entirety).

A monoclonal antibody directed against a determined antigen can, for example, be obtained by:

a) immortalizing lymphocytes obtained from the peripheral blood of an animal previously immunized with a determined antigen, with an immortal cell and preferably with myeloma cells, in order to form a hybridoma,

b) culturing the immortalized cells (hybridoma) formed and recovering the cells producing the antibodies having the desired specificity.

Alternatively, the use of a hybridoma cell is not required. Accordingly, monoclonal antibodies can be obtained by a process comprising the steps of:

a) cloning into vectors, especially into phages and more particularly filamentous bacteriophages, DNA or cDNA sequences obtained from lymphocytes especially peripheral blood lymphocytes of an animal (suitably previously immunized with determined antigens),

b) transforming prokaryotic cells with the above vectors in conditions allowing the production of the antibodies,

c) selecting the antibodies by subjecting them to antigen-affinity selection,

d) recovering the antibodies having the desired specificity.

Methods for immunizing camelids, cloning the VHH repertoire of B cells circulating in blood (Chomezynnski et al., 1987), and isolation of antigen-specific VHHs from immune (Arbabi-Ghahroudi et al., 1997) and nonimmune (Tanha et al 2002) libraries using phage, yeast, or ribosome display are known (WO92/01047, Nguyen et al., 2001 and Harmsen et al., 2007. These references are herein incorporated by reference in their entirety.

Antibody fragments such as the scFv and Fv fragments can be isolated and expressed in E. coli (Miethe et al., 2013, Skerra et al., 1988 and Ward et al., 1989, herein incorporated by reference in their entirety).

Mutations can be made to the DNA or cDNA that encode polypeptides which are silent as to the amino acid sequence of the polypeptide, but which provide preferred codons for translation in a particular host. The preferred codons for translation of a nucleic acid in, e.g., E. coli and S. cerevisiae, are known.

Mutation of polypeptides can be achieved for example by substitutions, additions or deletions to a nucleic acid encoding the polypeptide. The substitutions, additions or deletions to a nucleic acid encoding the polypeptide can be introduced by many methods, including for example error-prone PCR, shuffling, oligonucleotide-directed mutagenesis, assembly PCR, PCR mutagenesis, in vivo mutagenesis, cassette mutagenesis, recursive ensemble mutagenesis, exponential ensemble mutagenesis, site-specific mutagenesis (Ling et al 1997, herein incorporated by reference in its entirety), gene reassembly, Gene Site Saturation Mutagenesis (GSSM), synthetic ligation reassembly (SLR) or a combination of these methods. The modifications, additions or deletions to a nucleic acid can also be introduced by a method comprising recombination, recursive sequence recombination, phosphothioate-modified DNA mutagenesis, uracil-containing template mutagenesis, gapped duplex mutagenesis, point mismatch repair mutagenesis, repair-deficient host strain mutagenesis, chemical mutagenesis, radiogenic mutagenesis, deletion mutagenesis, restriction-selection mutagenesis, restriction-purification mutagenesis, ensemble mutagenesis, chimeric nucleic acid multimer creation, or a combination thereof.

In particular, artificial gene synthesis may be used (Nambiar et al 1984, Sakamar et al., 1988, Wells et al., 1985 and Grundstrom et al., 1985, herein incorporated by reference in their entirety). A gene encoding a polypeptide can be synthetically produced by, for example, solid-phase DNA synthesis. Entire genes may be synthesized de novo, without the need for precursor template DNA. To obtain the desired oligonucleotide, the building blocks are sequentially coupled to the growing oligonucleotide chain in the order required by the sequence of the product. Upon the completion of the chain assembly, the product is released from the solid phase to solution, deprotected, and collected. Products can be isolated by high-performance liquid chromatography (HPLC) to obtain the desired oligonucleotides in high purity (Verma et al., 1998) Expression of immunoglobulin chain variable domains such as VHs and VHHs can be achieved using a suitable expression vector such as a prokaryotic cell such as bacteria, for example E. coli (for example according to the protocols disclosed in WO94/04678, which is incorporated herein by reference and detailed further below). Expression of immunoglobulin chain variable domains such as VHs and VHHs can also be achieved using eukaryotic cells, for example insect cells, CHO cells, Vero cells or suitably yeast cells such as yeasts belonging to the genera Aspergillus, Saccharomyces, Kluyveromyces, Hansenula or Pichia. Suitably S. cerevisiae is used (for example according to the protocols disclosed in WO94/025591, which is incorporated herein by reference and detailed further below).

Specifically, VHHs can be prepared according to the methods disclosed in WO94/04678 using E. coli cells by a process comprising the steps of:

a) cloning in a Bluescript vector (Agilent Technologies) a DNA or cDNA sequence coding for the VHH (for example obtained from lymphocytes of camelids or produced synthetically) optionally including a His-tag,

b) recovering the cloned fragment after amplification using a 5′ primer specific for the VHH containing an XhoI site and a 3′ primer containing the SpeI site having the sequence TC TTA ACT AGT GAG GAG ACG GTG ACC TG (SEQ ID NO: 13),

c) cloning the recovered fragment in phase in the Immuno PBS vector (Huse et al., 1989, herein incorporated by reference in its entirety) after digestion of the vector with XhoI and SpeI restriction enzymes,

d) transforming host cells, especially E. coli by transfection with the recombinant Immuno PBS vector of step c,

e) recovering the expression product of the VHH coding sequence, for instance by affinity purification such as by chromatography on a column using Protein A, cation exchange, or a nickel-affinity resin if the VHH includes a His-tag.

Alternatively, immunoglobulin chain variable domains such as VHs and VHHs are obtainable by a process comprising the steps of:

a) obtaining a DNA or cDNA sequence coding for a VHH, having a determined specific antigen binding site,

b) amplifying the obtained DNA or cDNA, using a 5′ primer containing an initiation codon and a HindIII site, and a 3′ primer containing a termination codon having a XhoI site,

c) recombining the amplified DNA or cDNA into the HindIII (position 2650) and XhoI (position 4067) sites of a plasmid pMM984 (Merchlinsky et al., 1983, herein incorporated by reference in its entirety),

d) transfecting permissive cells especially NB-E cells (Faisst et al., 1995, herein incorporated by reference in its entirety) with the recombinant plasmid,

e) recovering the obtained products.

Further, immunoglobulin chain variable domains such as VHHs or VHs can be produced using E. coli or S. cerevisiae according to the methods disclosed in Frenken et al., 2000 and WO99/23221 (herein incorporated by reference in their entirety) as follows:

After taking a blood sample from an immunised llama and enriching the lymphocyte population via Ficoll (a neutral, highly branched, high-mass, hydrophilic polysaccharide which dissolves readily in aqueous solutions-Pharmacia) discontinuous gradient centrifugation, isolating total RNA by acid guanidium thiocyanate extraction (Chomezynnski et al., 1987), and first strand cDNA synthesis (e.g. using a cDNA kit such as RPN 1266 (Amersham)), DNA fragments encoding VHH and VH fragments and part of the short or long hinge region are amplified by PCR using the specific primers detailed on pages 22 and 23 of WO99/23221. Upon digestion of the PCR fragments with PstI and HindIII or BstEII, the DNA fragments with a length between about 300 and 450 bp are purified via agarose gel electrophoresis and ligated in the E. coli phagemid vector pUR4536 or the episomal S. cerevisiae expression vector pUR4548, respectively. pUR4536 is derived from pHEN (Hoogenboom et al., 1991, herein incorporated by reference in its entirety) and contains the lacl^(q) gene and unique restriction sites to allow the cloning of the llama VHH and VH genes. pUR4548 is derived from pSY1 (Harmsen et al., 1993, herein incorporated by reference in its entirety). From this plasmid, the BstEII site in the leu2 gene is removed via PCR and the cloning sites between the SUC2 signal sequence and the terminator are replaced in order to facilitate the cloning of the VH/VHH gene fragments. The VH/VHHs have the c-myc tag at the C-terminus for detection. Individual E. coli JM109 colonies are transferred to 96 well microtiter plates containing 150 ml 2TY medium supplemented with 1% glucose and 100 mg L⁻¹ ampicillin. After overnight growth (37 degrees C.), the plates are duplicated in 2TY medium containing 100 mg L⁻¹ ampicillin and 0.1 mM IPTG. After another overnight incubation and optionally freezing and thawing, cells are centrifuged and pelleted and the supernatant can be used in an ELISA. Individual S. cerevisiae colonies are transferred to test tubes containing selective minimal medium (comprising 0.7% yeast nitrogen base, 2% glucose, supplemented with the essential amino acids and bases) and are grown for 48 h at 30 degrees C. Subsequently, the cultures are diluted ten times in YPGal medium (comprising 1% yeast extract, 2% bacto peptone and 5% galactose). After 24 and 48 h of growth, the cells are pelleted and the culture supernatant can be analysed in an ELISA. Absorbance at 600 nm (OD600) is optionally measured.

Further, immunoglobulin chain variable domains such as VHNVHHs can be produced using S. cerevisiae using the procedure as follows:

Isolate a naturally-occurring DNA sequence encoding the VH/VHH or obtain a synthetically produced DNA sequence encoding the VH/VHH, including a 5′-UTR, signal sequence, stop codons and flanked with SacI and HindIII sites (such a synthetic sequence can be produced as outlined above or for example may be ordered from a commercial supplier such as Geneart (Life Technologies)).

Use the restriction sites for transfer of the VH/VHH gene to the multi-copy integration (MCI) vector pUR8569 or pUR8542, as follows. Cut the DNA sequence encoding the VHH optionally contained within a shuttle vector, cassette or other synthetic gene construct and the MCI vector with SacI and HindIII using: 25 ul VHH DNA (Geneart plasmid or MCI vector), 1 ul SacI, 1 ul HindIII, 3 ul of a suitable buffer for double digestion such as NEB buffer 1 (New England Biolabs) overnight at 37 degrees C. Run 25 ul of digested DNA encoding the VHH and 25 ul of digested MCI vector on a 1.5% agarose gel with 1×TAE buffer and then perform gel extraction for example using QIAquick Gel Extraction Kit (Qiagen)). Set-up a ligation of digested MCI vector and digested DNA encoding the VH/VHH as follows: 100 ng vector, 30 ng VHH gene, 1.5 ul 10×ligase buffer, 1 ul T4 DNA ligase, and ddH₂O. Then perform ligation overnight at 16 degrees C.

Next transform the E. coli cells. For chemical competent XL-1 blue cells, thaw 200 ul heat competent XL-1 blue cells and add 5 ul ligation mix on ice for about 30 minutes followed by heat shock for 90 seconds at 42 degrees C. Then add 800 ul Luria-Bertani low salt medium supplemented with 2% glucose and recover cells for 2 hours at 37 degrees C. Plate cells on Luria-Bertani agar and ampicillin (100 ug/ml) plates and keep overnight at 37 degrees C. For electro competent TG1 E. coli cells, use an electroporation cuvette. In the electroporation cuvette: thaw 50 ul electro competent TG1 cells and 1 ul ligation mix on ice for about 15 minutes. Place the cuvette in the holder and pulse. Add 500 ul of 2TY medium and recover cells for 30 minutes at 37 degrees C. Plate 100 ul of cells on Luria-Bertani, agar, containing ampicillin (100 ug/ml) and 2% glucose plates. Keep plates at 37 degrees C. overnight.

After cloning of the VH/VHH gene into E. coli as detailed above, S. cerevisiae can be transformed with the linearized MCI vector. Before transformation is carried out, some steps are performed: (i) the DNA should be changed from circular to linear by digestion or else the DNA cannot be integrated into the yeast genome and (ii) the digested DNA should be cleaned of impurities by ethanol precipitation. Also, during the transformation process, the yeast cells are made semi-permeable so the DNA can pass the membrane.

Preparation for yeast transformation: perform a HpaI digestion of the midi-prep prepared from the selected E. coli colony expressing the VH/VHH gene as follows. Prepare a 100 ul solution containing 20 ng of midi-prep, 5 ul HpaI, 10 ul of appropriate buffer such as NEB4 buffer (BioLabs), and ddH₂O.

Cut the DNA with the HpaI at room temperature overnight. Next perform an ethanol precipitation (and put to one side a 5 ul sample from HpaI digestion). Add 300 ul ethanol 100% to 95 ul HpaI digested midiprep, vortex, and spin at full speed for 5 minutes. Carefully decant when a pellet is present, add 100 ul of ethanol 70%, then spin again for 5 minutes at full speed. Decant the sample again, and keep at 50-60 degrees C. until the pellet is dry. Re-suspend the pellet in 50 ul ddH₂O. Run 5 ul on a gel beside the 5 ul HpaI digested sample. Yeast transformation: prepare YNBglu plates. Use 10 g agar+425 ml water (sterilised), 25 ml filtered 20x YNB (3.35 g YNB (yeast nitrogen base) in 25 ml sterilized H₂O) and 50 ml sterile 20% glucose and pour into petri dishes. Pick one yeast colony from the masterplate and grow in 3 ml YPD (Yeast Extract Peptone Dextrose) overnight at 30 degrees C. Next day prepare about 600 ml YPD and use to fill 3 flasks with 275 ml, 225 ml and 100 ml YPD. Add 27.5 ul yeast YPD culture to the first flask and mix gently. Take 75 ml from the first flask and put this in the second flask, mix gently. Take 100 ml from the second flask and put in the third one, mix gently. Grow until reaching an OD660 of between 1 and 2. Divide the flask reaching this OD over 4 Falcon tubes, ±45 ml in each. Spin for 2 minutes at 4200 rpm. Discard the supernatant. Dissolve the pellets in two Falcon tubes with 45 ml H₂O (reducing the number of tubes from 4 to 2). Spin for 2 minutes at 4200 rpm. Dissolve the pellets in 45 ml H₂O (from 2 tubes to 1). Spin for 2 minutes at 4200 rpm. Gently dissolve the pellets in 5 ml lithium acetate (LiAc) (100 mM), and spin for a few seconds. Carefully discard some LiAc, but retain over half of the LiAc in the tube. Vortex the cells, boil carrier DNA for 5 minutes and quickly chill in ice-water. Add to a 15 ml tube containing: 240 ul PEG, 50 ul cells, 36uLiAc (1M), 25 ul carrier DNA, 45 ul ethanol precipitated VH/VHH. Mix gently after each step (treat the blank sample the same, only without ethanol precipitated VH/VHH). Incubate for 30 minutes at 30 degrees C., gently invert the tube 3-4 times, then heat shock for 20-25 minutes at 42 degrees C. Spin up to 6000 rpm for a brief time. Gently remove the supernatant and add 250 ul ddH₂O and mix. Streak all of it on an YNBglu plate until plates are dry and grow for 4-5 days at 30 degrees C. Finally, prepare YNBglu plates by dividing plates in 6 equal parts, number the parts 1 to 6, inoculate the biggest colony and streak out number 1. Repeat for other colonies from big to small from 1 to 6. Grow at 30 degrees C. for 3-4 days large until colonies are produced. The VH/VHH clones are grown using glucose as a carbon source, and induction of VH/VHH expression is done by turning on the Galactose-7-promoter by adding 0.5% galactose. Perform a 3 mL small scale culture to test the colonies and choose which one shows the best expression of the VH or VHH. This colony is then used in purification.

Purification: the VH/VHH is purified by cation exchange chromatorgraphy with a strong anion resin (such as Capto S). On day 1, inoculate the selected yeast colony expressing the VH/VHH in 5 ml YPD medium (YP medium+2% glucose) and grow the cells in 25 mL sealed sterile tubes at 30 degrees C. overnight (shaking at 180 rpm). On day 2, dilute the 5 ml overnight culture in 50 mL freshly prepared YP medium+2% glucose+0.5% galactose, grow the cells in 250 ml aerated baffled flasks at 30 degrees C. for two nights (shaking at 180 rpm). On day 4, spin the cells down in a centrifuge at 4200 rpm for 20 min. Cation exchange purification step using a strong anion resin: adjust the pH of the supernatant containing the ligand to 3.5. Wash 0.75 ml resin (+/−0.5 mL slurry) per of 50 mL supernatant with 50 mL of ddH₂O followed by three washes with binding buffer. Add the washed resin to the supernatant and incubate the suspension at 4 degrees C. on a shaker for 1.5 hours. Pellet the resin-bound VH/VHH by centrifugation at 500 g for 2 minutes and wash it with wash buffer. Decant supernatant and re-suspend the resin with 10 mL of binding buffer. Put a filter in a PD-10 column, pour the resin in the column and let the resin settle for a while, then add a filter above the resin. Wait until all binding buffer has run through. Elute the VH/VHH with 6×0.5 ml elution buffer. Collect the elution fractions in eppendorf tubes. Measure the protein concentration of the 6 eluted fractions with a Nanodrop. Pool the fractions that contain the VHH and transfer the solution into a 3,500 Da cutoff dialysis membrane. Dialyze the purified protein solution against 3 L of PBS overnight at 4 degrees C. On day 5, dialyze the purified protein solution against 2 L of fresh PBS for an additional 2 hours at 4 degrees C. Finally, calculate the final concentration by BCA.

Although discussed in the context of the VH/VHH, the techniques described above could also be used for scFv, Fab, Fv and other antibody fragments if required.

Multiple antigen-binding fragments (suitably VHNVHHs) can be fused by chemical cross-linking by reacting amino acid residues with an organic derivatising agent such as described by Blattler et al., 1985 (herein incorporated by reference in its entirety). Alternatively, the antigen-binding fragments may be fused genetically at the DNA level i.e. a polynucleotide construct formed which encodes the complete polypeptide construct comprising one or more antigen-binding fragments. One way of joining multiple antigen-binding fragments via the genetic route is by linking the antigen-binding fragment coding sequences either directly or via a peptide linker. For example, the carboxy-terminal end of the first antigen-binding fragment may be linked to the amino-terminal end of the next antigen-binding fragment. This linking mode can be extended in order to link antigen-binding fragments for the construction of tri-, tetra-, etc. functional constructs. A method for producing multivalent (such as bivalent) VHH polypeptide constructs is disclosed in WO 96/34103 (herein incorporated by reference in its entirety).

Suitably, the polypeptide can be produced in a fungus such as a yeast (for example, S. cerevisiae) comprising growth of the fungus on a medium comprising a carbon source wherein 50-100 wt % of said carbon source is ethanol, according to the methods disclosed in WO02/48382. Large scale production of VHH fragments in S. cerevisiae is described in Thomassen et al., 2002 (herein incorporated by reference in its entirety).

In one aspect of the invention there is provided a method of making a composition of the invention comprising the step of expressing a polynucleotide encoding a TNF-alpha binding polypeptide using a suitable host and expressing a polynucleotide encoding an IL-6R binding polypeptide in a suitable host and adding both polypeptides to a composition. In a further aspect of the invention there is provided a method of making a construct of the invention comprising the step of expressing a polynucleotide encoding a construct of the invention using a suitable host.

The present invention will now be further described by means of the following non-limiting examples.

EXAMPLES Example 1: Potency of a TNF-Alpha Binding Polypeptide, ID-38F, Compared to TNF-Alpha Binding Polypeptides of the Prior Art (L929 Assay)

The neutralising potency of ID-38F (SEQ ID NO: 8), an immunoglobulin chain variable domain which binds to TNF-alpha, was compared in one and the same L929 assay (for further details, see above under ‘TNF-alpha binding polypeptides’) to that of the following anti-TNF-alpha polypeptides of the prior art:

TNF1 (a VHH disclosed in WO2006122786, therein SEQ ID NO: 52)

TNF3 (a VHH disclosed in WO2006122786, therein SEQ ID NO: 60)

TNF30 (a VHH disclosed in WO2006122786, therein SEQ ID NO: 96)

VHH#3E (a VHH disclosed in WO2004041862, therein SEQ ID NO: 4)

Adalimumab (commercially available human monoclonal antibody, trade name HUMIRA®)

Materials

L929 cells (10⁴ cells/well)

96-well plates (Costar)

DMEM (Invitrogen) supplemented with Pen/Strep+2 mM L-glutamine

Human TNF-alpha (Invitrogen) concentration: 500 pg/ml

Actinomycin D concentration (Sigma): 0.75 ug/mL

ID-38F purified from S. cerevisiae

ID-38F Flag-His tagged purified from E. coli

Adalimumab

TNF1, TNF3, TNF30, VHH#4E purified from E. coli with Flag-His tags

Range of dilutions: 5 pM-30 nM (1:3 dilutions)

Incubation times: 23 h

Alamar Blue cell viability reagent (Invitrogen, DAL1100): 10 uL/well

3% SDS

Microplate reader (Fluostar Optima) (OD590 nm)

Method

10⁴ L929 cells/well in 100 ul were plated on day 0 in 96 well micro-plates (Costar) in DMEM complete medium and stored over night at 37° C. and 5% CO₂. On day 1 serial dilutions 1:3 (in DMEM+Act.D) for each purified VHH/Ab were set up at double the assay concentrations (with volumes sufficient for triplicates) starting from a top concentration of 60 nM. 165 uL of each dilution were then diluted 1:1 with 165 uL of hTNF-alpha 2×(1 ng/mL) prepared in DMEM+Act.D. 0.9 mL of TNF 2× were diluted with 0.9 mL of cell medium+Act. D to have the TNF only control in the assay. The medium was removed from each well of the assay microplates and the cells were incubated with 100 uL of each TNF+VHH dilution, CM+act. D or TNF only control. After 23 h of incubation at 37° C. and 5% CO₂, 10 ul of Alamar Blue were added to each well, the cells were incubated for 2 h at 37° C. and 5% CO₂, and 50 ul of 3% SDS were subsequently added to each well. The plates were then read at 590 nm.

Results

The resultant neutralisation curves (produced with GraphPad Prism, using 4 parameter non-linear regression curve) are shown in FIG. 1. EC50 values are shown in Table 1.

TABLE 1 Anti-TNF-alpha polypeptide EC50 (nM) TNF1 0.751 TNF3 0.631 TNF30 0.420 VHH#3E 1.110 ID38F-Flag-His (E. coli-produced) 0.102 ID38F (S. cerevisiae-produced) 0.127 Adalimumab 0.091

It can be seen from FIG. 1 and Table 1 that VHH#3E was the least potent anti-TNF-alpha polypeptide in neutralising human soluble TNF-alpha-induced cytotoxicity in L929 cells. ID-38F (both E. coli- and S. cerevisiae-produced) had an approximately 4 fold-1 log lower EC50 than that of the prior art anti-TNF-alpha VHHs.

Example 2: Potency of a TNF-Alpha Binding Polypeptide, ID-38F (ELISA Assay)

The neutralising activities of adalimumab and ID-38F in a TNFR-2—TNF-alpha ELISA were compared.

An ELISA plate was coated overnight with 1.51 pg/ml TNFR-2 (Enbrel) in PBS overnight at 4° C. The plate was then washed and blocked in 1% BSA for >1 h at RT before being used. Adalimumab and ID-38F were made up in 1% BSA and 0.5% human AB serum in PBS at 9.258 nM and 20 nM respectively. From these solutions a further 10 dilutions were made for each antibody using a 1:1.6875 dilution factor and 1% BSA, 0.5% human AB serum in PBS as a diluent. All the antibody dilutions were mixed 1:1 with 5 ng/ml TNF-alpha and incubated for 1 h before adding to the ELISA plate and incubate at RT for 2 h. The plate was washed and incubated with 0.4 pg/ml biotinylated anti TNFα (P31A) for 2 h before an incubation with Extravidin-HRP (1/2000). Finally, the plate was washed again and 100 μl/well of TMB were added. Colour development was stopped by adding 50 μl/well of 0.5M H₂SO₄ and OD450 nm measurements were taken using a BMG Labtek Fluostar Omega plate reader.

TNFR-2—TNFα binding inhibition curves for adalimumab and ID-38F were generated from the data using a robust fit of a 4 parameter, non-linear curve fit in GraphPad Prism (not shown). These analyses also generated the EC50 data for both antibodies (see Table 2 below).

TABLE 2 Adalimumab, pM ID-38F, pM EC50 213.5 382.8

Example 3: Intestinal Protease Resistance of a TNF-Alpha Binding Polypeptide, ID-38F

Experiments were performed to investigate the stability of ID-38F when exposed to enzymes of the GIT (present in mouse small intestinal supernatant and human faecal supernatant). The contents of the small intestines from seven C57BL/6 male mice were removed with 0.9% saline, combined, homogenised and centrifuged. The resulting supernatant was removed, aliquoted and frozen.

Human faecal samples were turned into slurries with addition of 1×PBS. The slurries were then pooled, centrifuged and the supernatants removed, aliquoted and stored at −80 degrees C. This process removes the faecal matrix, including any cellular material.

Digests

ID-38F stock solution at 250 ug/mL was prepared in 0.34% (3400 ug/mL) BSA. To 55.2 uL of faecal or small intestinal supernatant on ice, 4.8 ul of ID-38F was added and mixed by vortexing. 25 uL was immediately removed and mixed with 25 uL of ice-cold protease stop solution (undigested control), and frozen at −80 degrees C. Aliquots of 25 ul were placed in wells of a polycarbonate thin-walled PCR plate and incubated for 17 h or 7 h respectively at 37 degrees C. After incubation, the digested ID-38F samples were placed on ice and 25 uL of ice-cold protease stop solution was added to each tube. The samples were frozen at −80 degrees C. before assay.

ELISA

ID-38F was diluted in 1% BSA+1× protease inhibition solution, mixed 1:1 with 5 ng/mL h-TNF-alpha, and incubated at RT for 1 h. The ID-38F and TNF-alpha mixture was then loaded onto blocked ELISA plates coated with 1 ug/mL etanercept and incubated for 2 hours with shaking at RT. The plates were washed 4× with PBST, dried by tapping and incubated with the biotinylated rabbit anti human-TNF-alpha polyclonal antibody (50 uL/well, 0.3 ug/mL) for 1 hour with shaking at RT. After 1 h, the plates were washed and incubated with mAvidin-HRP (50 uL/well, 1/1000 dilution) with shaking at RT for 30 min. The plates were then washed and dried as before and developed using 100 uL TMB. Standard curves (in PBS) were run alongside the non-digested samples. The top concentration of ID-38F used in the standard curve was 100 ng/mL.

Data Analyses

After digestion, the ID-38F concentration was measured using a TNFR2-interference ELISA. In this assay, ID-38F is mixed with TNF-alpha. The remaining level of TNF-alpha is then measured. The concentration of ID-38F is inferred from the amount of TNF-alpha inhibited from binding the TNFR2 receptor that is bound to the ELISA plate. Raw OD450 values were adjusted with blank readings taken from wells containing 1% BSA only. Standard curves were plotted using Graphpad Prism using non-linear regression to fit four-parameter curves. ID-38F concentration in the test samples were calculated in Graphpad Prism using the standard curve. The % survival was calculated by dividing the average ID-38F concentration in the 0-time point wells by the average ID-38F concentration for a single time point. The standard error of the ratio of two means was calculated.

Results

ID-38F achieved approximately 20% survival after 16 hours incubation in mouse small intestinal supernatant and approximately 45% survival after 16 hours incubation in human faecal supernatant. ID-38F is therefore remarkably stable to intestinal proteases.

Example 4: Binding Affinity for TNF-Alpha of a TNF-Alpha Binding Polypeptide, ID-38F

TNF-alpha was coupled to a switchSENSE® chip via covalently linked DNA to perform molecular biophysical analysis. Humira Fab or ID-38F were then flowed over the chip. Under these conditions, the K_(on) values were virtually identical (ID-38F appears to have slightly higher affinity than Humira Fab). Using this format (TNF-alpha bound to the chip), an off rate was obtained for the Humira Fab. However, due to its small size, reliable data could not be obtained for ID-38F in this orientation. Instead, ID-38F was coupled to the chip and TNF-alpha was flowed over the chip. When the off-rate data for Humira Fab (with TNF on the chip) and TNF-alpha (with ID-38F on the chip) were compared, the off rates were again very similar. It was confirmed that TNF-alpha was trimeric at the point of measurement (i.e. when being bound by Humira Fab or ID-38F). The affinity measurements are provided below in Table 3. The Kd of ID-38F was ascertained to be 16.8 pM.

TABLE 3 Assay k_(on)(10⁶ M⁻¹s⁻¹) k_(off)(10⁻⁵s⁻¹) Kd(pM) orientation Detection signal Humira    32 ± 1 (n = 3) 3.7 ± 0.9 (n = 3)  1.2 ± 0.4 TNFa Dynamic Response immob. Humira    10 ± 1 (n = 5) 5.1 ± 0.3 (n = 3)  5.1 ± 0.7 TNFa Dynamic Response Fab immob. ID-38F 2.5 ± 0.1 (n = 5) 4.2 ± 2.0 (n = 3) 16.8 ± 8.6 ID-38F Fluorescence immob. ID-38F 8.1 ± 0.2 (n = 3) not measurable No data TNFa Fluorescence immob.

Example 5: Administration of ID-38F to Humans-Polypeptide Concentration at the Ileal-Caecal Junction and in Faeces

Polypeptide Concentration at the Ileal-Caecal Junction

The aim of this study was to demonstrate that ID-38F (a TNF-alpha binding ICVD), incorporated into an enterically-coated pharmaceutical composition, is delivered at high concentrations to the ileal-caecal junction in man, a major site for Crohn's disease and the proximal site of Crohn's disease lesions in the intestine of many patients.

Four human volunteers, fitted with terminal ileostomy bags each received a single oral dose of 1665 mg ICVD, formulated into mini-tabs inside size 00 capsules (9 capsules in total). In these otherwise healthy individuals, the entire contents of the terminal ileum drains into the detachable external bag. At each hourly time point post-dosing, the fitted bag containing the total ileal effluent was removed, frozen and a new bag was fitted. Ileostomy samples were collected in this manner every hour for a period of 12 hours post dosing. Following this time, ileostomy samples were collected every four hours up to 24 hours post dosing. A pre-dosing sample (day −1) was also taken as a control. Any partially dissolved mini-tablets observed in the bags were removed prior to analysis such that only fully soluble ICVD was analysed. The ICVD was extracted from the ileal fluid and concentrations of active ICVD were determined by functional ELISA, assuming that 1 g ileal fluid is equivalent to 1 mL liquid volume.

The data revealed high concentrations of active ICVD present in the ileostomy bags, in the range 200 nM up to 1 mM. In addition, high concentrations were observed over several hours of bag changes for each subject (see Table 4).

TABLE 4 Hour post ICVD concentration in ileal Subject dose fluid (nM) 31001 2 406350 31001 3 305560 31001 4 791 31002 2 32780 31002 3 1130000 31002 4 792060 31002 5 81750 31002 6 12780 31002 7 1300 31002 8 422 31002 9 1410 31002 10 7520 31002 11 10080 31002 12 9210 31002 16 6980 31003 3 1060000 31003 4 496030 31003 5 7080 31003 8 46110 31003 9 75480 31003 10 16030 31003 11 72940 31003 12 15870 31003 16 881 31004 2 126190 31004 3 235 31004 4 11110 31004 5 3770 31004 6 6730 ICVD was not detected in any of the predose (Day −1) samples from any subject.

In summary, a sustained and high concentration of ID-38F was achieved at the ileal-caecal junction in these human volunteers.

Polypeptide Concentration in Faeces

Healthy male subjects aged 18-45 were dosed orally with a single dose of either 62, 555, 1665 or 4995 mg of ID-38F ICVD, delivered in the enterically-coated pharmaceutical composition described above. Each single dose per subject was administered between 8:30 to 12:00 on day 1. Faecal samples were collected pre dose (either on day −1, or prior to dosing on day 1) and at all available times post dosing up to the morning of day 4 (the end of the study). ICVD was extracted from the faeces and concentrations of active ICVD were determined by functional ELISA, assuming that Ig faeces is equivalent to 1 mL liquid volume and that the polypeptide is uniformly distributed in the faeces.

High concentrations in the range 180 nM to 724 pM were obtained in the faeces of subjects (see Table 5).

TABLE 5 Faecal mg sample dose collection Pre or post Subject ID ICVD day dose [ICVD] in faeces (nM) 11001 62 −1 PRE DOSE 0 11001 1 POST DOSE 1013 13001 555 −1 PRE DOSE 0 13001 2 POST DOSE 1052 13003 555 −1 PRE DOSE 0 13003 1 POST DOSE 1938 13003 2 POST DOSE 1511 14002 1665 −1 PRE DOSE 0 14002 1 POST DOSE 5491 14002 2 POST DOSE 558 14004 1665 −1 PRE DOSE 0 14004 2 POST DOSE 27532 14006 1665 −1 PRE DOSE 0 14006 2 POST DOSE 62579 15001 4995 −1 PREDOSE 0 15001 1 POST DOSE 10047 15001 2 POST DOSE 135285 15001 3 POST DOSE 330 15004 4995 −1 PREDOSE 0 15004 3 POST DOSE 273 15005 4995 1 PRE DOSE 0 15005 1 POST DOSE 724684 15005 2 POST DOSE 258703 15005 3 POST DOSE 3536 15006 4995 −1 PRE DOSE 0 15006 1 POST DOSE 57120 15006 2 POST DOSE 358 15006 2 POST DOSE 186

Anti-TNF agents that are used clinically to treat Crohn's disease, such as adalimumab (Humira) and infliximab (Remicade), are administered either by intravenous infusion or subcutaneous injection. Ungar et al. (2016) state that trough serum levels of 56-83 nM (8-12 pg/mL) for adalimumab and 42-70 nM (6-10 pg/mL) for infliximab are required to achieve mucosal healing in 80%-90% of patients with IBD, and that this could be considered as a “therapeutic window”.

Concentrations of anti-TNF-alpha ICVD delivered to the ileal-caecal junction and recovered in the faeces of human volunteers during the clinical work in this section were significantly higher than these levels and are thus predicted to be efficacious as a treatment for Crohn's disease. This assumes that gut luminal concentrations of anti-TNF-alpha ICVD are comparable to serum concentrations of marketed anti-TNF agents with respect to access/penetration to the gut mucosa and sub-mucosa. However, it has been demonstrated in further experimental work (not shown) that this anti-TNF-alpha ICVD, dosed orally in DSS colitis mice, is able to penetrate to the lamina propia where it is resident for several hours, despite a lack of target (TNF) engagement in mice.

These results demonstrate successful oral delivery of therapeutic levels of ICVD from the ileal-caecal junction to the anus.

Example 6: Potency of an IL-6R Binding Polypeptide, ID-123V (a Variant of ID-142V), Compared to an IL-6R Binding Polypeptide of the Prior Art, 20A11

The inhibitory potency and efficacy (maximal inhibition) of E. coli-produced ID-123V (an ICVD which binds to IL-6R, SEQ ID NO: 34) and tocilizumab (a commercially available anti-IL-6R antibody with the trade name ACTEMRA®) were confirmed in vitro in the gp130 ELISA, TF-1 cell and M1 cell functional assays measuring responses mediated via human IL-6R. The potency of ID-123V and tocilizumab in these assays is shown in Tables 6.1 to 6.3. The assays use the standard protocols provided above. The gp130 assay uses a final assay concentration of 10 ng/mL IL-6R and 50 ng/mL IL-6.

TABLE 6.1 gp130 ELISA assay gp130 ELISA Construct EC50 nM ID-123V 0.498 Tocilizumab 1.831 20A11 0.220

TABLE 6.2 TF-1 cell assay TF-1 cell assay EC50 nM Construct (5 ng/ml IL-6) ID-123V 4.50 Tocilizumab 1.12 20A11 0.56

TABLE 6.3 M1 cell assay M1 cellular Construct assay EC50 nM ID-123V 4.20 Tocilizumab 5.36

In summary, it can be seen that ID-123V has high potency in the various assays performed.

Example 7: Binding Affinity and Specificity for Human IL-6R of an IL-6R Binding Polypeptide, ID-123V

The binding kinetics of ID-123V were compared against tocilizumab in a Biacore study. The ICVD was fixed to the Biacore sensor plate and soluble human IL-6R was flowed over the plate to detect binding. Tocilizumab and ID-123V had similar Kds of 0.39 and 1.1 nM, respectively. The results indicate that ID-123V binds strongly to IL-6R.

Example 8: Potency of an IL-6R Binding Polypeptide, ID-142V

The potencies of ID-142V (SEQ ID NO: 16), ID-123V (SEQ ID NO: 34) and tocilizumab were assessed in the M1 cell assay (the M1 cell assay is dependent on IL-6 trans signalling).

It can be seen that the ICVD ID-123V detailed in the examples above is equivalent to ID-142V except for ID-123V being produced in E. coli and therefore lacking the E1D mutation.

Rapidly growing M1 cells were suspended in RPMI+3% FCS medium at 106 cells/ml. Fifty microliters of cell suspension were added to wells on the assay plates. ID-123V was produced in E. coli and contained a C-terminal Flag, His tag, whilst ID-142V contained no tag and was produced in yeast. As a result, the N-terminus for the yeast produced ID-142V was Asp (D), whilst the N-terminus of ID-123V was Glu (E). For each antibody a range of concentrations were prepared from 600 nM solutions using a 1:2.667 dilution factor, using RPMI+3% FCS as a diluent. All antibody dilutions were mixed with 120 ng/ml IL-6 and 600 ng/ml IL-6 (both in RPMI+3% FCS) in a 1:1:1 ratio, then 50 μl of each mixture were added to the assay plates (1:1), giving a final IL-6 and IL-6R concentration of 100 ng/ml and 20 ng/ml IL-6 and IL-6R respectively. Plates were incubated for 5 days, then viable cell mass was measured by incubating with 10μl/well Alamar blue for 5 h and measuring 620 nm emission fluorescence.

Data for % inhibition of the IL-6+IL-6R response are shown in Table 7 below. In summary, tocilizumab potency was similar to ID-142V.

TABLE 7 Binding polypeptide EC50, nM ID-123V 2.31 ID-142V 4.05 Tocilizumab 4.16

Example 9: Intestinal Protease Resistance of IL-6R Binding Polypeptides ID-123V and ID-142V, Compared to an IL-6R Binding Polypeptide of the Prior Art

Experiments were performed to investigate the stability of ID-123V, ID-142V and an IL-6R binding polypeptide of the prior art (20A11) when exposed to enzymes of the GIT (present in mouse small intestinal supernatant and human faecal supernatant).

Assessment in Mouse Small Intestinal Supernatant and Human Faecal Extract Assays

ID-123V, ID-142V and 20A11 were tested for survival in mouse small intestinal supernatant and human faecal extract assays. Survival was measured by a gp130 plate ELISA.

A mouse small intestinal supernatant assay was performed with 7 hours' digestion and a human faecal extract assay was performed with 16 hours' digestion. % survival was established for the ICVDs as follows in Table 8.

TABLE 8 Mouse small Human intestinal faecal supernatant extract 7 h 16 h % ICVD % survival survival ID-123V 85 95 ID-142V 47 92 20A11 0 0

It can be seen that ID-123V and ID-142V are highly protease resistant ICVDs, while 20A11 is highly unstable in protease matrices.

Resistance to Gastrointestinal Matrix Metalloproteases

Levels of activated matrix metalloproteases (MMPs) are increased in the inflamed mucosa of patients with intestinal bowel disease. These MMPs are able to digest native human IgG and therapeutic agents that contain a human IgG scaffold (Biancheri et al, 2015). In the case of the anti-TNF-alpha therapy etanercept, this digestion causes a significant reduction in TNF-alpha neutralising potency. To confirm that ID-123V is resistant to MMPs, ID-123V was incubated for 18 hours in the presence of activated recombinant human MMP3 and MMP12.

Following incubation, ID-123V was fully potent at neutralising IL-6R, as measured using an IL-6-slL-6R-gp130 functional ELISA. However, after the same incubation time, MMP3 and MMP12 digested full-length etanercept and tocilizumab (anti-IL-6R) to smaller fragments, as measured by Western blotting.

Mouse Digestive Transit and Survival

Results of the in vitro studies described above showed that ID-123V was highly resistant to inactivation by proteases present in a supernatant extract prepared from mouse small intestinal contents. A subsequent study was performed to investigate the stability of ID-123V during passage through the gastrointestinal system of the mouse. ID-123V was formulated with a further, unrelated ICVD in a milk and bicarbonate mixture to protect against denaturation at low pH and digestion by pepsin in the stomach. Following administration of the ICVDs to mice by oral gavage, concentrations of the ICVDs in stomach, small intestine, caecum and colon were determined at 3 hours post-dosing. In addition, the ICVD concentration in faecal pellets collected at hourly intervals was measured.

Four mice were tested. The transit and excretion of the ICVDs in faeces varied between the mice tested. In three of the mice, ID-123V was detected in faeces between 2 and 4 hours after dosing, suggesting that ID-123V can survive transit through the mouse GI tract.

Examining the concentrations of ID-123V in each compartment at 3 hours post-dose revealed ID-123V in the stomach and small intestine. It is expected therefore that ID-123V will have good stability in the human intestinal tract.

Example 10: Investigation of the Inhibitory Effects of a TNF-Alpha Binding Polypeptide and an IL-6R Binding Polypeptide, Administered Separately and in Combination, on the Phosphorylation of Signalling Proteins in Ex Vivo Cultured IBD Tissue

The TNF-alpha binding polypeptide used in the experiments detailed below is the ICVD ID-38F (SEQ ID NO: 8). The IL-6R binding polypeptide used in the experiments detailed below is the ICVD ID-142V (SEQ ID NO: 16).

Infliximab is effective for the treatment of IBD. Infliximab is thought to act primarily by neutralising the biological activity of TNF leading to inhibition of the downstream pro-inflammatory effects of the cytokine. Activation of the many different cell types present in diseased tissue by TNF and secondary inflammatory mediators involves multiple receptor signalling pathways resulting in the phosphorylation of receptors, protein kinases and transcription factors. Experiments have shown that (i) patterns of protein phosphorylation are altered in IBD vs normal intestinal tissue and that (ii) patterns of phosphorylation are sensitive to inhibitors of specific pro-inflammatory mechanisms.

The effects of a TNF-alpha binding polypeptide and an IL-6R binding polypeptide (the ICVDs ID-38F and ID-142V, respectively), delivered both individually and in combination, on the phosphorylation of signalling proteins in intestinal mucosal tissue from IBD patients was investigated as detailed below.

IBD Tissue

Endoscopic colonic mucosal biopsies were obtained from patients with active Inflammatory Bowel Disease (IBD). Patient characteristics are listed in Table 9.

TABLE 9 Details of IBD Patients, Disease Presentation and Medication Sex; birth Patient # Presentation/Biopsy Medication year CD2241 /colon Azathioprine M; 1976 CD2244 /colon Azathioprine, Budesonide M; 1982 CD2250 /colon No meds; (on Humira 1 M; 1992 year ago) CD2256 /terminal ileum No meds M; 1985 UC2245 mild pancolitis Mesalazine oral and topical M; 1955 UC2249 mayo 1-2 colitis left- No meds F; 1985 sided

Organ Culture

Mucosal biopsies taken from active IBD cases (CD & UC) with inflamed mucosa were cultured (one biopsy per well) in 24-well plates (VWR International, Lutterworth, UK) in 300 μl serum-free HL-1 medium (Cambrex BioScience, Wokingham, UK) supplemented with glutamine, 100 pg/ml penicillin, 100 pg/ml streptomycin, 50 ug/mL gentamicin and cultured at 37° C., 5% CO₂. Biopsies were cultured for 24 h with the addition of the following antibodies; ID-38F or ID-142V each at a final concentration of 250 nM, ID-38F plus ID-142V each at a concentration of 250 nM and ID-2A (irrelevant control ICVD) 500 nM. Details of the antibodies are summarised in Table 10. Supernatants and tissue samples collected at the end of the experiment were snap-frozen and stored at −70° C.

TABLE 10 Details of Antibodies and Treatment Groups Well Time Antibody Activity Assay 1 24 h ID-2A Unrelated ICVD Negative Control 2 24 h ID-38F Anti-TNF ICVD Mono-specific 3 24 h ID-142V Anti-IL-6R ICVD Mono-specific 4 24 h ID-38F + ID- Anti-TNF + Anti-IL-6R Combined Specificity 142V ICVDs

Signalling Arrays and Data Analysis

For the analysis of phospho-protein content the IBD tissue samples were thawed, lysed in RIPA buffer (Sigma-Aldrich, St. Louis, Mo.) supplemented with phosphatase inhibitor cocktail 2 (Sigma-Aldrich) and protease inhibitor cocktail (Sigma-Aldrich), both at 1%. Protein concentrations of the lysates were determined by the Bio-Rad protein assay (Bio-Rad Laboratories, Hemel Hempstead, UK) and samples diluted to 1.0 mg/ml in Array Diluent Buffer.

-   1. The phosphorylation status of receptor tyrosine kinases and     signalling molecules was determined by using PathScan RTK signalling     arrays (Cell Signalling Technology, Danvers, Mass.). The array kit     allows for the simultaneous detection of 28 receptor tyrosine     kinases and 11 important signalling nodes, when phosphorylated at     tyrosine or other residues. -   2. A total of 150 ug of protein from each biopsy tissue lysate was     probed onto each array. For each CD and UC patient, the lysates     prepared from the set of antibody-treated biopsies (ID-2A, ID-38F,     ID-142V and ID-38F+ID-142V) were analysed on the same slide. -   3. The chemiluminescent signals of all arrays were detected on X-ray     films, and the pixel intensities were measured using ImageJ     software. -   4. For each antibody treatment, the phosphoprotein signals obtained     from each of the four different patient biopsies (n=4 CD lysates)     were used to calculate mean+/−SD pixel intensity values that are     shown in FIG. 2 (shown in ‘AU’-arbitrary units). FIG. 2 is split     over three sections, with different phosphoproteins displayed in     each section. -   5. To account for differences between patients the pixel array data     obtained for each of the experimental treatments were normalised     against the pixel values obtained for the corresponding patient and     ID-2A treatment control. Percentage inhibition of control values     were calculated and presented in FIG. 3. Values for each treatment     (ID-38F, ID-142V and ID-38F+ID-142V) were derived from the analysis     of lysates from four different CD patients. -   6. For comparison the treatments were repeated using inflamed biopsy     tissue from two patients with ulcerative colitis. The mean+/−SD     pixel intensity values obtained for each treatment (ID-2A, ID-38F,     ID-142V and ID-38F+ID-142V) of n=2; UC lysates were used to     calculate mean+/−SD pixel intensity values that are shown in FIG. 4

Results

Results presented in FIG. 2 show the levels of phosphorylation detected on the phospho-array for each of the TK receptor and signalling proteins. The mean pixel intensity values were calculated for each phosphoprotein on the array (data from n=4 Crohn's biopsies) and for each phosphoprotein the values obtained for each treatment have been plotted together.

Inhibition of Protein Phosphorylation in Inflamed Crohn's Disease Tissue—Treatment with a TNF-Alpha Binding Protein and an IL-6R Binding Protein Separately

When compared with the ID-2A controls, the pixel intensities measured for the Crohn's biopsies treated with either ID-38F or ID-142V showed that both ICVDs inhibited the phosphorylation levels of all the signalling proteins on the array (see FIG. 2). When values for the experimental treated samples were normalised to the respective ID-2A Crohn's tissue control (FIG. 3), the average percentage inhibition (n=4 CD patients) measured for all phosphoproteins on the array following ID-38F treatment was 47% (range 30% to 100%), while the average percentage inhibition following ID-142V treatment was slightly greater 59% (range 43% to 100%). Many of these proteins including CSF-1R, Tyro-3, Axl, Akt, ZAP-70, Lck, Stat1 and Stat3 are known to have functions involved the regulation of inflammatory cells including macrophages and T cells that contribute to the immunopathology of Crohn's disease. The changes in phosphorylation are therefore consistent with the established anti-inflammatory effects of known TNF and IL-6R-neutralising antibodies.

Inhibition of Protein Phosphorylation in Inflamed Crohn's Disease Tissue—Treatment with a TNF-Alpha Binding Protein and an IL-6R Binding Protein Simultaneously

In general, the inhibitory effect of ID-38F and ID-142V combined exceeded that achieved by treatment with each ICVD individually.

Inhibition of Protein Phosphorylation in Inflamed Ulcerative Colitis Tissue—Treatment with a TNF-Alpha Binding Protein and an IL-6R Binding Protein Separately

The pixel intensity values for individual phosphoproteins and the pattern of intensities on the arrays found in the control ID-2A-treated UC biopsy tissue samples (average values for n=2 UC patients) were generally quite similar to those detected in the Crohn's tissue (FIG. 4). However, the levels of phosphorylation of EphB4, Tyro3, Axl and VEGFR2 appeared to be higher while phosphorylation of Ret was lower in UC compared with CD tissue.

Treatment of UC tissue for 24 h with ID-38F inhibited the phosphorylation of most of the proteins detected on the array, with a pattern broadly similar to that seen in Crohn's tissue. Interestingly, the inhibition by either ID-38F or ID-142V of a set of phosphoproteins that included VEGFR2/KDR, Akt/PKB/Rac Thr308, Akt/PKB/Rac Ser473, p44/42 MAPK (ERK1/2), S6 ribosomal protein, c-Abl, IRS-1, Zap-70, Src, Lck, Stat1 and Stat3 was relatively weak.

Inhibition of Protein Phosphorylation in Inflamed Ulcerative Colitis Tissue—Treatment with a TNF-Alpha Binding Protein and an IL-6R Binding Protein Simultaneously

When the treatments were combined, phosphorylation levels of most of these proteins were suppressed close to baseline.

In summary, treatment with an anti-TNF-alpha binding polypeptide and an anti-IL-6R binding polypeptide together was surprisingly more effective than treatment with each binding polypeptide alone.

Example 11: Investigation of the Inhibitory Effects of a TNF-Alpha Binding Polypeptide and an IL-6R Binding Polypeptide, Administered Separately and in Combination, on the Production of Cytokines in Ex Vivo Cultures of IBD Tissue

TNF-alpha and IL-6 are important for the activation of inflammatory processes that contribute to the pathology and chronicity of IBD. Many of these effects rely on the regulation of complex cytokine networks that in turn control the different cellular processes involved in inflammation and immune-regulation. In this experiment it was investigated whether the TNFalpha- and/or IL-6R-neutralising activities of ID-38F and ID-142V, alone and in combination, can inhibit the production of cytokines that are thought to be important for the development of inflammation in IBD.

IBD Tissue

Endoscopic colonic mucosal biopsies were obtained from patients with active Inflammatory Bowel Disease (IBD). Patient characteristics are listed in Table 11.

TABLE 11 Details of IBD Patients, Disease Presentation and Medication Presentation/ Date Patient # Biopsy Medication M/F CD2241 /colon Azathioprine M; 1976 CD2244 /colon Azathioprine, Budesonide M; 1982 CD2250 /colon No meds; (on Humira 1 M; 1992 year ago) CD2254 /ileum Azathioprine, prednisolone F; 1958 CD2256 /terminal No meds M; 1985 ileum CD2259 /colon Azathioprine M; 1975

Organ Culture

Mucosal biopsies (four biopsies per patient) were taken from six patients with active Crohn's disease. The inflamed mucosa biopsies were cultured (one biopsy per well) in 24-well plates (VWR International, Lutterworth, UK) in 300 μl serum-free HL-1 medium (Cambrex BioScience, Wokingham, UK) supplemented with glutamine, 100 pg/ml penicillin, 100 pg/ml streptomycin, 50 ug/mL gentamicin and cultured at 37° C., 5% CO₂. The set of biopsies (×4) from each patient were cultured for 24 h with the addition of the following antibodies; ID-38F or ID-142V each at a final concentration of 250 nM, ID-38F plus ID-142V each at a concentration of 250 nM and ID-2A (irrelevant control ICVD) at a concentration of 500 nM. Details of the ICVDs are summarised in Table 12. Supernatants and tissue samples collected at the end of the experiment were snap-frozen and stored at −70° C.

TABLE 12 Details of Antibodies and Treatment Groups Well Time Antibody Activity Assay 1 24 h ID-2A Unrelated ICVD Negative Control 2 24 h ID-38F Anti-TNF ICVD Mono-specific 3 24 h ID-142V Anti-IL-6R ICVD Mono-specific 4 24 h ID-38F + ID- Anti-TNF + Anti-IL-6R Combined Specificity 142V ICVDs

Multiplexed Cytokine Assays

The 24 h culture supernatants recovered from each of the four ICVD-treated biopsies (ID-2A, ID-38F, ID-142V and ID-38F+ID-142V) were analysed for each of the six CD patients. The frozen culture supernatants were thawed and analysed for levels of IFN-gamma, TNF-alpha, IL-10, IL-17A, IL-1-beta, IL-6 and IL-8 using multiplexed cytokine assay kits and R&D Systems MagPix technology.

-   -   1. Samples were diluted 1:2 in reagent diluent.     -   2. Standards (custom mix by R&D Systems) were re-suspended and         1:3 serial dilutions were prepared.     -   3. The pre-mixed micro-particle cocktail (custom mix by R&D) was         prepared with reagent diluent.     -   4. Additions were made of 50 ul/well of standards and samples;         both in duplicates, plus 50 ul of micro-particle cocktail/well.     -   5. The plate was sealed and incubated for 2 h at RT on a shaker     -   6. The plate was then attached to a magnet and washed using a         multichannel pipette 3× with wash buffer.     -   7. 50 ul of biotin Ab cocktail (custom mix by R&D) was added per         well. The plate was resealed and incubated on a shaker for 1 h         at RT.     -   8. The wash step was repeated wash 3× using the magnet.     -   9. 50 ul of Streptavidin-PE mix was added/well and the plate         incubated for a further 30 min at RT on a shaker.     -   10. After washing 3x, the microparticles were resuspended by         adding 100 ul wash buffer/well, followed by incubation on a         shaker for 2 minutes.     -   11. The plate was read using a Luminex analyser. The MagPix         machine used was calibrated with R&D's calibration kit before         each run.

Assay data obtained for cytokine standards were used to generate standard curves; cytokine concentrations present in the culture supernatants were then calculated from the respective standard curves.

Data Analysis

The 24 h culture supernatants recovered from the set of four ICVD-treated biopsies (ID-2A, ID-38F, ID-142V and ID-38F+ID-142V) were analysed for each of the six CD patients. The cytokine concentrations were determined and the mean values (Mean+/−Standard Deviation) were calculated using the results obtained from the set of six donors. Results are summarised in FIG. 5.

Differences in the levels of inflammation and/or cellular involvement in biopsies taken from different patients could potentially result in different levels of spontaneous cytokine production between patients. To allow treatment effects to be more clearly identified the cytokine concentration value obtained for each experimental treatment was normalised to the value obtained for the corresponding patient ID-2A treatment control. The normalised % control values obtained for each cytokine (IFN-gamma, TNF-alpha, IL-10, IL-17A, IL-1-beta, IL-6 and IL-8) measured for each patient were then combined and the mean values (Mean+/−SD; n=6 CD patients) calculated. Normalised (% control) cytokine values obtained for the different treatments (ID-38F/ID-2A; ID-142V/ID-2A; Combined ID-38F+ID-142V/ID-2A) are presented in FIG. 6.

Results

The levels of spontaneous production of six different pro-inflammatory cytokines (IFN-gamma, TNF-alpha, IL-17A, IL-1-beta, IL-6 and IL-8), and of IL-10 (which has anti-inflammatory activities), are presented in FIG. 5.

When compared with the production levels of cytokines measured for the control ID-2A treated tissue, both ID-38F- and ID-142V-treatments resulted in some inhibition of each of the six pro-inflammatory cytokines. The spontaneous production of IL-1-beta, IL-17 and TNF-alpha were inhibited by ID-38F and ID-142V most strongly. The control-normalised cytokine data presented in FIG. 6 also show that both ID-38F- and ID-142V-treatments were inhibitory.

When ID-38F and ID-142V treatments were combined, the spontaneous production of each of the inflammatory cytokines IFN-gamma, TNF-alpha, IL-17A, IL-1-beta, IL-6 and IL-8 was inhibited to a greater extent than that achieved with either ICVD individually.

In contrast to the inhibitory effects of these ICVDs on production of the pro-inflammatory cytokines, treatment with ID-38F, ID-142V or the combination increased production of the anti-inflammatory cytokine IL-10 relative to the control (ID-2A).

In summary, treatment with an anti-TNF-alpha binding polypeptide and an anti-IL-6R binding polypeptide together was surprisingly more effective than treatment with each binding polypeptide alone.

Example 12: Production and Cleavage of a Heterobihead Construct Comprising ID-38F and ID-142V Linked by a Labile Linker and a Heterobihead Construct Comprising ID-38F and ID-142V Linked by a Non-Labile Linker

This experiment demonstrates the liberation by trypsin of ID-38F and ID-142V from a heterobihead construct in which these ICVDs are linked by a labile peptide linker and also the stability to trypsin of a heterobihead construct comprising ID-38F and ID-142V ICVDs linked by a non-labile peptide linker.

Heterobihead constructs comprising ID-38F and ID-142V, linked by either labile or non-labile peptide linkers, were expressed in S. cerevisiae. ID-9K and ID-10K in this example were designed for secretion using the invertase (SUC2) signal sequence, whereas ID-11K was fused to the yeast mating factor alpha leader sequence at the N-terminus. These constructs were of the following formats, shown in Table 13:

TABLE 13 Construct Target(s) Monomers Linker ID-9K TNF- ID-38F/ GGGGSKGGGGS (residues 87-335 of alpha/ ID-142V (SEQ ID  SEQ ID NO: 19) IL-6R NO: 32) ID-10K IL-6R/ ID-142V/ GGGGSKGGGGS (residues 87-335 of TNF- ID-38F (SEQ ID  SEQ ID NO: 20) alpha NO: 32) ID-11K TNF- ID-38F/ GGGGSGGGGS (residues 87-354 of alpha/ ID-142V GGGGSGGGGS SEQ ID NO: 21) IL-6R GGGGSGGGGS (SEQ ID  NO: 33)

Residues 1-86 of these sequences are the export signal sequence. Residues 87-335 of SEQ ID NO: 19 and residues 87-335 SEQ ID NO: 20 are the ID-9K and ID-10K polypeptide constructs, respectively. Residues 87-354 of SEQ ID NO: 21 is the ID-11K polypeptide construct.

ID9K and ID10K were cloned into the SacI/BsteII sites of episomal expression vector pYQVQ07, which employs a similar technology to that described for plasmids pUR4547 (as described in EP 1002861 A1) and pSY1 (Harmsen et al., 1993). pYQVQ07 is a shuttle vector, capable of replication in E. coli and S. cerevisiae for episomal expression. ID11K was cloned into the SacI/HindIII sites of integration vector pUR9013. pUR9013 encodes S. cerevisiae DNA that facilitates high copy number integration into the chromosomal rDNA locus, following linearization of the plasmid, via a similar mechanism to that described by Lopes et al. 1989. Cloning into both vectors introduces a galactose-inducible promoter upstream of the expression cassette. Expression, and full secretion into the supernatant, from S. cerevisiae was achieved via galactose induction. Finally, ID9K and ID10K constructs were purified using Protein A affinity resin (GE) and ID11K was purified using Capto S cation exchange resin (GE) and dialysed into ix PBS.

To test the lability of the peptide linkers, these constructs were incubated in the presence of trypsin-agarose beads (Sigma, T4019). After time intervals of 0, 15, 30, 45 (ID-11K only) and 60 minutes of incubation at 37° C. in a convection water bath, samples were taken. Equal volumes from each timepoint were analysed on a denaturing SDS-polyacrylamide gel. The gels were then stained with coomassie, destained and imaged by ImageQuant (GE). The quantity of intact constructs relative to cleaved constituent polypeptides can be assessed by comparing the corresponding bands in each time point lane. Images of the gels are shown in FIGS. 7 and 8, wherein st indicates a non-treated bihead standard (no exposure to trypsin beads), MW indicates molecular weight (kDa) and lanes correspond to 0, 15, 30, 45 and 60 minutes' incubation at 37° C. with trypsin beads. Time zero samples were kept on ice prior to sampling.

It can be seen from FIG. 7 that both ID-9K and ID-10K (molecular weights of around 28 kDa) had successfully liberated almost all of their constituent ICVD monomers (each having molecular weights of around 14 kDa) after 30 minutes of incubation with trypsin. ID-11K by contrast is fully stable to trypsin digestion over a 1 hour time period (FIG. 8).

Miscellaneous

All references referred to in this application, including patent and patent applications, are incorporated herein by reference to the fullest extent possible.

Throughout the specification and the claims which follow, unless the context requires otherwise, the word ‘comprise’, and variations such as ‘comprises’ and ‘comprising’, will be understood to imply the inclusion of a stated integer, step, group of integers or group of steps but not to the exclusion of any other integer, step, group of integers or group of steps.

The application of which this description and claims forms part may be used as a basis for priority in respect of any subsequent application. The claims of such subsequent application may be directed to any feature or combination of features described herein. They may take the form of product, composition, process, or use claims and may include, by way of example and without limitation, the following claims.

REFERENCES

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1. A composition comprising: (a) an antibody or antibody fragment that binds TNF-alpha, said antibody or said antibody fragment comprising three complementarity determining regions (CDR1-CDR3), wherein CDR1 comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO: 1, CDR2 comprises a sequence sharing 50% or greater sequence identity with SEQ ID NO: 2 and CDR3 comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO: 3; and (b) an antibody or antibody fragment that binds IL-6R, said antibody or said antibody fragment comprising three complementarity determining regions (CDR1-CDR3), wherein CDR1 comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO: 9, CDR2 comprises a sequence sharing 50% or greater sequence identity with SEQ ID NO: 10 and CDR3 comprises a sequence sharing 60% or greater sequence identity with SEQ ID NO:
 11. 2. The composition according to claim 1, wherein said antibody or said antibody fragment of (a) binds to TNF-alpha with a Kd of 10-7 M or less, and said antibody or said antibody fragment of (b) binds to IL-6R with a Kd of 10-7 M or less.
 3. The composition according to claim 1, wherein said antibody or said antibody fragment of (a) neutralizes human TNF-alpha cytotoxicity in an L929 assay with an EC50 of 1 nM or less, and said antibody or said antibody fragment of (b) neutralizes IL-6R in a standard gp130 ELISA assay with an EC50 of 1 nM or less.
 4. The composition according to claim 2, wherein said antibody or said antibody fragment of (a) neutralizes human TNF-alpha cytotoxicity in an L929 assay with an EC50 of 1 nM or less, and said antibody or said antibody fragment of (b) neutralizes IL-6R in a standard gp130 ELISA assay with an EC50 of 1 nM or less.
 5. The composition according to claim 1, wherein said antibody or said antibody fragment that binds TNF-alpha and said antibody or said antibody fragment that binds IL-6R are linked.
 6. The composition according to claim 5, wherein said antibody or said antibody fragment that binds TNF-alpha and said antibody or antibody fragment that binds IL-6R are linked by a protease-labile peptide linker.
 7. The composition according to claim 6, wherein the protease-labile peptide linker comprises a K and/or R residue.
 8. The composition according to claim 1, wherein said antibody or antibody fragment of (a) and said antibody or antibody fragment of (b) retain neutralization activity when exposed to one or more proteases present in the small or large intestine.
 9. The composition according to claim 1 wherein the composition is suitable for oral administration.
 10. The composition according to claim 1, wherein the composition comprises an enteric coating.
 11. The composition according to claim 9, wherein the composition comprises an enteric coating.
 12. A pharmaceutical composition comprising the composition according to claim 1 and a pharmaceutically acceptable excipient.
 13. A method of treating an autoimmune disease and/or an inflammatory disease comprising administering to a person in need thereof a therapeutically effective amount of the composition according to claim
 1. 14. The method according to claim 13, wherein the autoimmune disease and/or inflammatory disease is inflammatory bowel disease and/or mucositis.
 15. The method according to claim 14, wherein the inflammatory bowel disease is ulcerative colitis or Crohn's disease.
 16. The method according to claim 13, wherein the composition is administered orally. 